Canonical Allele Identifier: CA1674890179
Gene:

Linked Data

dbSNP Id: rs144168014

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817543G>C , CM000668.2:g.155817543G>C GRCh38
NC_000006.11:g.156138677G>C , CM000668.1:g.156138677G>C GRCh37
NC_000006.10:g.156180369G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943142.1:n.79+24124G>C
XR_943146.1:n.552-2873C>G
XR_001744423.1:n.606-2873C>G
XR_001744424.1:n.79+24124G>C