Canonical Allele Identifier: CA834982489
Gene:

Linked Data

dbSNP Id: rs1473397598
MyVariant Identifiers: chr7:g.148258042G>T (hg19) chr7:g.148560950G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148560950G>T , CM000669.2:g.148560950G>T GRCh38
NC_000007.13:g.148258042G>T , CM000669.1:g.148258042G>T GRCh37
NC_000007.12:g.147888975G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928099.1:n.300+7150C>A
XR_928100.1:n.433+7150C>A
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