Canonical Allele Identifier: CA13769800
Gene:

Linked Data

dbSNP Id: rs7307780
gnomAD v2: 12-76220618-C-T
gnomAD v3: 12-75826838-C-T
gnomAD v4: 12-75826838-C-T
MyVariant Identifiers: chr12:g.76220618C>T (hg19) chr12:g.75826838C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.75826838C>T , CM000674.2:g.75826838C>T GRCh38
NC_000012.11:g.76220618C>T , CM000674.1:g.76220618C>T GRCh37
NC_000012.10:g.74506885C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749214.2:n.379-131863G>A
XR_002957419.1:n.379-131863G>A
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