Canonical Allele Identifier: CA357497352

Gene: ADH7

Linked Data

• dbSNP Id: rs1721623128
• MyVariant Identifiers: chr4:g.100341694G>C (hg19) ; chr4:g.99420537G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420537G>C , CM000666.2:g.99420537G>C	GRCh38
NC_000004.11:g.100341694G>C , CM000666.1:g.100341694G>C	GRCh37
NC_000004.10:g.100560717G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.821C>G MANE Select	ENSP00000414254.2:p.Thr274Ser
ENST00000209665.8:c.857C>G	ENSP00000209665.4:p.Thr286Ser
ENST00000437033.6:c.821C>G	ENSP00000414254.2:p.Thr274Ser
ENST00000476959.5:c.881C>G	ENSP00000420269.1:p.Thr294Ser
ENST00000482593.5:c.650C>G	ENSP00000420613.1:p.Thr217Ser
NM_000673.4:c.857C>G	NP_000664.2:p.Thr286Ser
NM_001166504.1:c.881C>G	NP_001159976.1:p.Thr294Ser
NM_000673.7:c.821C>G MANE Select	NP_000664.3:p.Thr274Ser
NM_001166504.2:c.881C>G	NP_001159976.1:p.Thr294Ser