Canonical Allele Identifier: CA834982454

Gene:

Linked Data

• dbSNP Id: rs1355840019
• MyVariant Identifiers: chr7:g.148257997T>C (hg19) ; chr7:g.148560905T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.148560905T>C , CM000669.2:g.148560905T>C	GRCh38
NC_000007.13:g.148257997T>C , CM000669.1:g.148257997T>C	GRCh37
NC_000007.12:g.147888930T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_928099.1:n.300+7195A>G
XR_928100.1:n.433+7195A>G