Canonical Allele Identifier: CA3672285
Gene: BTN3A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26374343G>A , CM000668.2:g.26374343G>A GRCh38
NC_000006.11:g.26374571G>A , CM000668.1:g.26374571G>A GRCh37
NC_000006.10:g.26482550G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_007047.5:c.981G>A MANE Select NP_008978.2:p.Ser327=
ENST00000377708.7:c.981G>A MANE Select ENSP00000366937.2:p.Ser327=
NM_001197246.2:c.981G>A NP_001184175.1:p.Ser327=
NM_001197247.2:c.981G>A NP_001184176.1:p.Ser327=
NM_001197247.3:c.981G>A NP_001184176.1:p.Ser327=
NM_001197248.2:c.912G>A NP_001184177.1:p.Ser304=
NM_001197248.3:c.912G>A NP_001184177.1:p.Ser304=
NM_001197249.2:c.855G>A NP_001184178.1:p.Ser285=
NM_001197249.3:c.855G>A NP_001184178.1:p.Ser285=
NM_007047.4:c.981G>A NP_008978.2:p.Ser327=
ENST00000356386.6:c.981G>A ENSP00000348751.2:p.Ser327=
ENST00000377708.6:c.981G>A ENSP00000366937.2:p.Ser327=
ENST00000396934.7:c.912G>A ENSP00000380140.3:p.Ser304=
ENST00000396948.5:c.981G>A ENSP00000380152.1:p.Ser327=
ENST00000508906.6:c.855G>A ENSP00000442687.1:p.Ser285=
ENST00000524682.5:n.614G>A
ENST00000527422.5:c.981G>A ENSP00000432138.1:p.Ser327=
ENST00000532294.1:n.334G>A
ENST00000604202.1:n.1651G>A
XM_005248827.2:c.981G>A XP_005248884.1:p.Ser327=
XM_005248827.4:c.981G>A XP_005248884.1:p.Ser327=
XM_005248831.2:c.780G>A XP_005248888.1:p.Ser260=
XM_005248831.4:c.780G>A XP_005248888.1:p.Ser260=
XM_005248832.2:c.780G>A XP_005248889.1:p.Ser260=
XM_005248832.4:c.780G>A XP_005248889.1:p.Ser260=
XM_006714979.2:c.996G>A XP_006715042.1:p.Ser332=
XM_006714979.4:c.996G>A XP_006715042.1:p.Ser332=
XM_006714980.2:c.996G>A XP_006715043.1:p.Ser332=
XM_006714980.4:c.996G>A XP_006715043.1:p.Ser332=
XM_006714981.2:c.996G>A XP_006715044.1:p.Ser332=
XM_006714981.4:c.996G>A XP_006715044.1:p.Ser332=
XM_006714982.2:c.870G>A XP_006715045.1:p.Ser290=
XM_006714982.4:c.870G>A XP_006715045.1:p.Ser290=
XM_011514267.1:c.996G>A XP_011512569.1:p.Ser332=
XM_011514267.3:c.996G>A XP_011512569.1:p.Ser332=
XM_011514268.1:c.996G>A XP_011512570.1:p.Ser332=
XM_011514269.1:c.870G>A XP_011512571.1:p.Ser290=
XM_011514269.3:c.870G>A XP_011512571.1:p.Ser290=
XM_011514270.1:c.699G>A XP_011512572.1:p.Ser233=
XM_011514270.3:c.699G>A XP_011512572.1:p.Ser233=
XM_011514271.1:c.699G>A XP_011512573.1:p.Ser233=
XM_011514271.2:c.699G>A XP_011512573.1:p.Ser233=
XM_017010211.1:c.981G>A XP_016865700.1:p.Ser327=
XM_017010212.1:c.981G>A XP_016865701.1:p.Ser327=
XM_017010213.2:c.870G>A XP_016865702.1:p.Ser290=
XM_017010214.2:c.855G>A XP_016865703.1:p.Ser285=
XM_017010215.2:c.699G>A XP_016865704.1:p.Ser233=
XM_017010216.2:c.654G>A XP_016865705.1:p.Ser218=
XM_017010217.2:c.573G>A XP_016865706.1:p.Ser191=