Canonical Allele Identifier: CA54965467
Gene:

Linked Data

dbSNP Id: rs183666542

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368818T>C , CM000664.2:g.122368818T>C GRCh38
NC_000002.11:g.123126394T>C , CM000664.1:g.123126394T>C GRCh37
NC_000002.10:g.122842864T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-24145T>C
XR_001739684.1:n.556-24145T>C