Canonical Allele Identifier: CA1439212808
Gene:

Linked Data

dbSNP Id: rs1395349197

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578174T>C , CM000666.2:g.12578174T>C GRCh38
NC_000004.11:g.12579798T>C , CM000666.1:g.12579798T>C GRCh37
NC_000004.10:g.12188896T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31168A>G
XR_001741374.1:n.254+44481A>G
XR_925406.3:n.140+31168A>G