Canonical Allele Identifier: CA101653647
Gene: ADH1B HGNC NCBI

Linked Data

dbSNP Id: rs897313007
gnomAD v2: 4-100242818-G-C
gnomAD v3: 4-99321661-G-C
gnomAD v4: 4-99321661-G-C
MyVariant Identifiers: chr4:g.100242818G>C (hg19) chr4:g.99321661G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99321661G>C , CM000666.2:g.99321661G>C GRCh38
NC_000004.11:g.100242818G>C , CM000666.1:g.100242818G>C GRCh37
NC_000004.10:g.100461841G>C NCBI36
NG_011435.1:g.4755C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000639454.1:c.19-2775C>G ENSP00000491622.1:n.19-2775C>G
Search 100 bp 5'
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