Canonical Allele Identifier: CA834982485
Gene:

Linked Data

dbSNP Id: rs1159406743
gnomAD v3: 7-148560946-C-T
gnomAD v4: 7-148560946-C-T
MyVariant Identifiers: chr7:g.148258038C>T (hg19) chr7:g.148560946C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148560946C>T , CM000669.2:g.148560946C>T GRCh38
NC_000007.13:g.148258038C>T , CM000669.1:g.148258038C>T GRCh37
NC_000007.12:g.147888971C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928099.1:n.300+7154G>A
XR_928100.1:n.433+7154G>A
Search 100 bp 5'
Search 100 bp 3'