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Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.5711488C>T , CM000666.2:g.5711488C>T
GRCh38
NC_000004.11:g.5713215C>T , CM000666.1:g.5713215C>T
GRCh37
NC_000004.10:g.5764116C>T
NCBI36
NG_008843.1:g.5292C>T
NG_015821.1:g.3061G>A
Transcript Alleles
HGVS
Amino-acid Change
ENST00000264956.11:c.108C>T
MANE Select
ENSP00000264956.6:p.Ala36=
ENST00000264956.10:c.108C>T
ENSP00000264956.6:p.Ala36=
ENST00000509451.1:c.108C>T
ENSP00000426774.1:p.Ala36=
NM_001306090.1:c.108C>T
NP_001293019.1:p.Ala36=
NM_001306092.1:c.108C>T
NP_001293021.1:p.Ala36=
NM_153717.2:c.108C>T
NP_714928.1:p.Ala36=
XM_006713865.2:c.108C>T
XP_006713928.1:p.Ala36=
XM_006713866.2:c.108C>T
XP_006713929.1:p.Ala36=
XM_011513419.1:c.108C>T
XP_011511721.1:p.Ala36=
XR_427473.2:n.298C>T
XR_427475.2:n.298C>T
XR_427476.2:n.298C>T
XR_924920.1:n.298C>T
XR_924921.1:n.298C>T
XR_924922.1:n.298C>T
XR_924923.1:n.298C>T
XR_924924.1:n.298C>T
XR_924925.1:n.298C>T
XR_924926.1:n.298C>T
XR_924927.1:n.298C>T
XR_924928.1:n.300C>T
XM_006713865.3:c.108C>T
XP_006713928.1:p.Ala36=
XM_006713866.3:c.108C>T
XP_006713929.1:p.Ala36=
XM_011513419.2:c.108C>T
XP_011511721.1:p.Ala36=
XM_017007883.2:c.108C>T
XP_016863372.1:p.Ala36=
XR_001741164.1:n.288C>T
XR_001741165.1:n.288C>T
XR_001741166.1:n.288C>T
XR_001741167.1:n.288C>T
XR_001741168.1:n.288C>T
XR_001741169.2:n.290C>T
XR_001741170.1:n.290C>T
XR_427473.3:n.288C>T
XR_427475.3:n.288C>T
XR_427476.3:n.288C>T
XR_924920.2:n.288C>T
XR_924921.2:n.288C>T
XR_924922.2:n.288C>T
XR_924924.2:n.288C>T
XR_924925.2:n.288C>T
XR_924926.2:n.288C>T
NM_153717.3:c.108C>T
MANE Select
NP_714928.1:p.Ala36=
NM_001306090.2:c.108C>T
NP_001293019.1:p.Ala36=
NM_001306092.2:c.108C>T
NP_001293021.1:p.Ala36=