Canonical Allele Identifier: CA234906724
Gene:

Linked Data

dbSNP Id: rs150722614
gnomAD v2: 12-28198268-C-G
gnomAD v3: 12-28045335-C-G
gnomAD v4: 12-28045335-C-G
MyVariant Identifiers: chr12:g.28198268C>G (hg19) chr12:g.28045335C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.28045335C>G , CM000674.2:g.28045335C>G GRCh38
NC_000012.11:g.28198268C>G , CM000674.1:g.28198268C>G GRCh37
NC_000012.10:g.28089535C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_931460.1:n.154-6377G>C
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