Canonical Allele Identifier: CA756632629
Gene:

Linked Data

dbSNP Id: rs1157626695

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127431651T>C , CM000664.2:g.127431651T>C GRCh38
NC_000002.11:g.128189227T>C , CM000664.1:g.128189227T>C GRCh37
NC_000002.10:g.127905697T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923313.1:n.1331+16A>G
XR_001739705.1:n.3607-3387A>G
XR_923313.2:n.4042+16A>G