Canonical Allele Identifier: CA235071419
Gene:

Linked Data

dbSNP Id: rs1025470604
gnomAD v3: 12-29961059-C-T
gnomAD v4: 12-29961059-C-T
MyVariant Identifiers: chr12:g.30113992C>T (hg19) chr12:g.29961059C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.29961059C>T , CM000674.2:g.29961059C>T GRCh38
NC_000012.11:g.30113992C>T , CM000674.1:g.30113992C>T GRCh37
NC_000012.10:g.30005259C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931473.1:n.314-18019G>A
XR_931474.1:n.314-18019G>A
XR_931475.1:n.135-18019G>A
XR_001749060.1:n.314-18019G>A
XR_001749061.1:n.314-18019G>A
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