Canonical Allele Identifier: CA1305906754
Gene:

Linked Data

dbSNP Id: rs1558902057

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168260470C>G , CM000664.2:g.168260470C>G GRCh38
NC_000002.11:g.169116980C>G , CM000664.1:g.169116980C>G GRCh37
NC_000002.10:g.168825226C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739763.1:n.912-4626C>G
XR_001739764.1:n.318-4626C>G
XR_001739765.1:n.436-4626C>G