Canonical Allele Identifier: CA553101598
Gene: ADH1B HGNC NCBI

Linked Data

dbSNP Id: rs931634180
gnomAD v2: 4-100242814-C-CT
gnomAD v3: 4-99321657-C-CT
gnomAD v4: 4-99321657-C-CT
MyVariant Identifiers: chr4:g.100242814_100242815insT (hg19) chr4:g.99321657_99321658insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99321657_99321658insT , CM000666.2:g.99321657_99321658insT GRCh38
NC_000004.11:g.100242814_100242815insT , CM000666.1:g.100242814_100242815insT GRCh37
NC_000004.10:g.100461837_100461838insT NCBI36
NG_011435.1:g.4758_4759insA

Transcript Alleles

HGVS Amino-acid change
ENST00000639454.1:c.19-2772_19-2771insA ENSP00000491622.1:n.19-2772_19-2771insA
Search 100 bp 5'
Search 100 bp 3'