Canonical Allele Identifier: CA834644125
Gene:

Linked Data

dbSNP Id: rs1429959411
MyVariant Identifiers: chr7:g.144841452C>A (hg19) chr7:g.145144359C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.145144359C>A , CM000669.2:g.145144359C>A GRCh38
NC_000007.13:g.144841452C>A , CM000669.1:g.144841452C>A GRCh37
NC_000007.12:g.144472385C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928090.1:n.1968-12576C>A
XR_928090.2:n.4143-12576C>A
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