Canonical Allele Identifier: CA1880524665
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128945523C= , CM000671.2:g.128945523C= GRCh38
NC_000009.11:g.131707802C= , CM000671.1:g.131707802C= GRCh37
NC_000009.10:g.130747623C= NCBI36
NG_017009.1:g.7211G= , LRG_744:g.7211G=
NG_033111.1:g.2831C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000482796.1:c.39-3666C= ENSP00000417556.2:n.39-3666C=