Canonical Allele Identifier: CA1674885525
Gene:

Linked Data

dbSNP Id: rs1778853823

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812291C>G , CM000668.2:g.155812291C>G GRCh38
NC_000006.11:g.156133425C>G , CM000668.1:g.156133425C>G GRCh37
NC_000006.10:g.156175117C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18872C>G
XR_943146.1:n.645-252G>C
XR_001744423.1:n.699-252G>C
XR_001744424.1:n.79+18872C>G