Canonical Allele Identifier: CA154409021
Gene:

Linked Data

dbSNP Id: rs1001928229
MyVariant Identifiers: chr7:g.13553910C>A (hg19) chr7:g.13514285C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.13514285C>A , CM000669.2:g.13514285C>A GRCh38
NC_000007.13:g.13553910C>A , CM000669.1:g.13553910C>A GRCh37
NC_000007.12:g.13520435C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745097.1:n.148-188031C>A
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Search 100 bp 3'