Canonical Allele Identifier: CA1439212711
Gene:

Linked Data

dbSNP Id: rs1577128466

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578091T>C , CM000666.2:g.12578091T>C GRCh38
NC_000004.11:g.12579715T>C , CM000666.1:g.12579715T>C GRCh37
NC_000004.10:g.12188813T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925406.1:n.106+31251A>G
XR_001741374.1:n.254+44564A>G
XR_925406.3:n.140+31251A>G