Canonical Allele Identifier: CA168906816
Gene:

Linked Data

dbSNP Id: rs944244717
MyVariant Identifiers: chr7:g.148257902A>G (hg19) chr7:g.148560810A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148560810A>G , CM000669.2:g.148560810A>G GRCh38
NC_000007.13:g.148257902A>G , CM000669.1:g.148257902A>G GRCh37
NC_000007.12:g.147888835A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928099.1:n.300+7290T>C
XR_928100.1:n.433+7290T>C
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