Canonical Allele Identifier: CA1880524668
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128945525A= , CM000671.2:g.128945525A= GRCh38
NC_000009.11:g.131707804A= , CM000671.1:g.131707804A= GRCh37
NC_000009.10:g.130747625A= NCBI36
NG_017009.1:g.7209T= , LRG_744:g.7209T=
NG_033111.1:g.2833A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000482796.1:c.39-3664A= ENSP00000417556.2:n.39-3664A=