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Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.121132962G= , CM000674.2:g.121132962G=
GRCh38
NC_000012.11:g.121570765G= , CM000674.1:g.121570765G=
GRCh37
NC_000012.10:g.120055148G=
NCBI36
NG_011471.2:g.5088G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000328963.10:c.-9G=
MANE Select
ENSP00000330696.6:n.-9G=
ENST00000261826.10:c.-9G=
ENSP00000261826.6:n.-9G=
ENST00000328963.9:c.-9G=
ENSP00000330696.6:n.-9G=
ENST00000535928.5:c.-9G=
ENSP00000439961.1:n.-9G=
ENST00000537312.5:c.-9G=
ENSP00000438586.1:n.-9G=
ENST00000539695.5:n.61G=
ENST00000545434.5:c.-9G=
ENSP00000445564.1:n.-9G=
NM_002562.5:c.-9G=
NP_002553.3:n.-9G=
NR_033948.1:n.135G=
NR_033949.1:n.135G=
NR_033950.1:n.135G=
NR_033951.1:n.135G=
NR_033952.1:n.135G=
NR_033953.1:n.144G=
NR_033954.1:n.135G=
NR_033955.1:n.135G=
NR_033956.1:n.135G=
XM_011538418.1:c.-9G=
XP_011536720.1:n.-9G=
XM_011538419.1:c.-152G=
XP_011536721.1:n.-152G=
XM_011538419.3:c.-152G=
XP_011536721.1:n.-152G=
XM_017019364.2:c.-522G=
XP_016874853.1:n.-522G=
XM_017019365.2:c.-353G=
XP_016874854.1:n.-353G=
XM_017019366.2:c.-689G=
XP_016874855.1:n.-689G=
XM_017019367.2:c.-520G=
XP_016874856.1:n.-520G=
XR_001749352.2:n.187-6121C=
XR_001749354.2:n.187-6121C=
NM_002562.6:c.-9G=
MANE Select
NP_002553.3:n.-9G=
NR_033948.2:n.87G=
NR_033949.2:n.87G=
NR_033950.2:n.87G=
NR_033951.2:n.87G=
NR_033952.2:n.87G=
NR_033953.2:n.87G=
NR_033954.2:n.87G=
NR_033955.2:n.87G=
NR_033956.2:n.87G=