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Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.238397556G= , CM000664.2:g.238397556G=
GRCh38
NC_000002.11:g.239306197G= , CM000664.1:g.239306197G=
GRCh37
NC_000002.10:g.238970936G=
NCBI36
NG_053055.1:g.82068G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000373327.5:c.1787G=
MANE Select
ENSP00000362424.4:p.Ser596=
ENST00000373327.4:c.1787G=
ENSP00000362424.4:p.Ser596=
ENST00000391993.7:c.1589G=
ENSP00000375851.3:p.Ser530=
ENST00000462122.1:n.798G=
ENST00000483951.1:n.135G=
NM_001139490.1:c.1589G=
NP_001132962.1:p.Ser530=
NM_015650.3:c.1787G=
NP_056465.2:p.Ser596=
XM_006712414.1:c.1586G=
XP_006712477.1:p.Ser529=
XM_011510944.1:c.1889G=
XP_011509246.1:p.Ser630=
XM_011510945.1:c.1850G=
XP_011509247.1:p.Ser617=
XM_011510946.1:c.1817G=
XP_011509248.1:p.Ser606=
XM_011510947.1:c.1757G=
XP_011509249.1:p.Ser586=
XM_011510948.1:c.1691G=
XP_011509250.1:p.Ser564=
XM_011510950.1:c.755G=
XP_011509252.1:p.Ser252=
XM_006712414.2:c.1586G=
XP_006712477.1:p.Ser529=
XM_011510944.2:c.1889G=
XP_011509246.1:p.Ser630=
XM_011510945.2:c.1850G=
XP_011509247.1:p.Ser617=
XM_011510946.2:c.1817G=
XP_011509248.1:p.Ser606=
XM_011510947.2:c.1757G=
XP_011509249.1:p.Ser586=
XM_011510948.2:c.1691G=
XP_011509250.1:p.Ser564=
XM_011510950.2:c.755G=
XP_011509252.1:p.Ser252=
XM_017003789.1:c.1886G=
XP_016859278.1:p.Ser629=
XR_001738696.1:n.1615G=
XR_001738697.1:n.1612G=
NM_015650.4:c.1787G=
MANE Select
NP_056465.2:p.Ser596=