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Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.43192310T>C , CM000670.2:g.43192310T>C
GRCh38
NC_000008.10:g.43047453T>C , CM000670.1:g.43047453T>C
GRCh37
NC_000008.9:g.43166610T>C
NCBI36
NG_009552.1:g.56862T>C
Transcript Alleles
HGVS
Amino-acid Change
ENST00000379644.9:c.1257T>C
MANE Select
ENSP00000368965.4:p.Tyr419=
ENST00000379644.8:c.1257T>C
ENSP00000368965.4:p.Tyr419=
ENST00000520678.1:n.190T>C
ENST00000521576.1:c.408T>C
ENSP00000429029.1:p.Tyr136=
ENST00000524016.5:c.361T>C
NM_152419.2:c.1257T>C
NP_689632.2:p.Tyr419=
XM_005273409.1:c.1257T>C
XP_005273466.1:p.Tyr419=
XM_005273410.1:c.1257T>C
XP_005273467.1:p.Tyr419=
XM_005273411.1:c.1065T>C
XP_005273468.1:p.Tyr355=
XM_005273412.2:c.1257T>C
XP_005273469.1:p.Tyr419=
NM_001363227.1:c.1257T>C
NP_001350156.1:p.Tyr419=
NM_001363228.1:c.1065T>C
NP_001350157.1:p.Tyr355=
NM_001363229.1:c.393T>C
NP_001350158.1:p.Tyr131=
XM_005273412.4:c.1257T>C
XP_005273469.1:p.Tyr419=
NM_152419.3:c.1257T>C
MANE Select
NP_689632.2:p.Tyr419=
NM_001363227.2:c.1257T>C
NP_001350156.1:p.Tyr419=
NM_001363228.2:c.1065T>C
NP_001350157.1:p.Tyr355=
NM_001363229.2:c.393T>C
NP_001350158.1:p.Tyr131=