Canonical Allele Identifier: CA168906793
Gene:

Linked Data

dbSNP Id: rs984892767
gnomAD v3: 7-148560763-A-C
gnomAD v4: 7-148560763-A-C
MyVariant Identifiers: chr7:g.148257855A>C (hg19) chr7:g.148560763A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148560763A>C , CM000669.2:g.148560763A>C GRCh38
NC_000007.13:g.148257855A>C , CM000669.1:g.148257855A>C GRCh37
NC_000007.12:g.147888788A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928099.1:n.300+7337T>G
XR_928100.1:n.433+7337T>G
Search 100 bp 5'
Search 100 bp 3'