Canonical Allele Identifier: CA357495913

Gene: ADH1B

Linked Data

• MyVariant Identifiers: chr4:g.100229018G>C (hg19) ; chr4:g.99307861G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99307861G>C , CM000666.2:g.99307861G>C	GRCh38
NC_000004.11:g.100229018G>C , CM000666.1:g.100229018G>C	GRCh37
NC_000004.10:g.100448041G>C	NCBI36
NG_011435.1:g.18555C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305046.13:c.1107C>G MANE Select	ENSP00000306606.8:p.Ile369Met
ENST00000639454.1:c.1107C>G	ENSP00000491622.1:p.Ile369Met
ENST00000305046.12:c.1107C>G	ENSP00000306606.8:p.Ile369Met
ENST00000506651.5:c.987C>G	ENSP00000425998.2:p.Ile329Met
ENST00000515694.4:n.3202C>G
ENST00000625860.2:c.987C>G	ENSP00000486614.1:p.Ile329Met
NM_000668.5:c.1107C>G	NP_000659.2:p.Ile369Met
NM_001286650.1:c.987C>G	NP_001273579.1:p.Ile329Met
NM_000668.6:c.1107C>G MANE Select	NP_000659.2:p.Ile369Met
NM_001286650.2:c.987C>G	NP_001273579.1:p.Ile329Met