Canonical Allele Identifier: CA2691057965
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104928288A>G , CM000671.2:g.104928288A>G GRCh38
NC_000009.11:g.107690569A>G , CM000671.1:g.107690569A>G GRCh37
NC_000009.10:g.106730390A>G NCBI36
NG_007981.1:g.4868T>C

Transcript Alleles

HGVS Amino-acid change
XR_930204.1:n.734+378A>G
XR_930204.2:n.115+378A>G