Canonical Allele Identifier: CA1127663272
Gene:

Linked Data

dbSNP Id: rs1826505966

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104928255T>C , CM000671.2:g.104928255T>C GRCh38
NC_000009.11:g.107690536T>C , CM000671.1:g.107690536T>C GRCh37
NC_000009.10:g.106730357T>C NCBI36
NG_007981.1:g.4901A>G

Transcript Alleles

HGVS Amino-acid change
XR_930204.1:n.734+345T>C
XR_930204.2:n.115+345T>C