Canonical Allele Identifier: CA102646738
Gene: ADH7 HGNC NCBI

Linked Data

dbSNP Id: rs994002919
MyVariant Identifiers: chr4:g.100342186G>C (hg19) chr4:g.99421029G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99421029G>C , CM000666.2:g.99421029G>C GRCh38
NC_000004.11:g.100342186G>C , CM000666.1:g.100342186G>C GRCh37
NC_000004.10:g.100561209G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.565-236C>G MANE Select ENSP00000414254.2:n.565-236C>G
ENST00000209665.8:c.601-236C>G ENSP00000209665.4:n.601-236C>G
ENST00000437033.6:c.565-236C>G ENSP00000414254.2:n.565-236C>G
ENST00000476959.5:c.625-236C>G ENSP00000420269.1:n.625-236C>G
ENST00000482593.5:c.394-236C>G ENSP00000420613.1:n.394-236C>G
NM_000673.4:c.601-236C>G NP_000664.2:n.601-236C>G
NM_001166504.1:c.625-236C>G NP_001159976.1:n.625-236C>G
NM_000673.7:c.565-236C>G MANE Select NP_000664.3:n.565-236C>G
NM_001166504.2:c.625-236C>G NP_001159976.1:n.625-236C>G
Search 100 bp 5'
Search 100 bp 3'