Canonical Allele Identifier: CA2384216349
Gene:

Linked Data

dbSNP Id: rs1981165200

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.27324119A>C , CM000683.2:g.27324119A>C GRCh38
NC_000021.8:g.28696438A>C , CM000683.1:g.28696438A>C GRCh37
NC_000021.7:g.27618309A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_430359.2:n.834+26380T>G
XR_937629.1:n.834+26380T>G
XR_937630.1:n.834+26380T>G
XR_430359.3:n.847+26380T>G
XR_937629.2:n.847+26380T>G