Canonical Allele Identifier: CA1653130379
Gene:

Linked Data

dbSNP Id: rs1771941114

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.105805141C>G , CM000668.2:g.105805141C>G GRCh38
NC_000006.11:g.106253016C>G , CM000668.1:g.106253016C>G GRCh37
NC_000006.10:g.106359709C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942835.1:n.510+24916G>C
XR_001744274.1:n.438+24916G>C
XR_001744275.1:n.337+24916G>C