Canonical Allele Identifier: CA800704723

Gene: ADH4

Linked Data

• dbSNP Id: rs1452953058
• gnomAD v3: 4-99124348-C-G
• gnomAD v4: 4-99124348-C-G
• MyVariant Identifiers: chr4:g.100045499C>G (hg19) ; chr4:g.99124348C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124348C>G , CM000666.2:g.99124348C>G	GRCh38
NC_000004.11:g.100045499C>G , CM000666.1:g.100045499C>G	GRCh37
NC_000004.10:g.100264522C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.*94G>C MANE Select	ENSP00000265512.7:n.*94G>C
ENST00000265512.11:c.*94G>C	ENSP00000265512.7:n.*94G>C
ENST00000508393.5:c.*94G>C	ENSP00000424630.1:n.*94G>C
ENST00000629236.2:c.*58G>C	ENSP00000486450.1:n.*58G>C
NM_000670.3:c.*94G>C	NP_000661.2:n.*94G>C
NM_000670.4:c.*94G>C	NP_000661.2:n.*94G>C
NM_001306171.1:c.*94G>C	NP_001293100.1:n.*94G>C
NM_001306172.1:c.*94G>C	NP_001293101.1:n.*94G>C
NR_037884.1:n.429-9207C>G
XR_938685.1:n.1576G>C
XR_938686.1:n.1567G>C
XR_938687.1:n.1440G>C
NM_000670.5:c.*94G>C MANE Select	NP_000661.2:n.*94G>C
NM_001306171.2:c.*94G>C	NP_001293100.1:n.*94G>C
NM_001306172.2:c.*94G>C	NP_001293101.1:n.*94G>C