Canonical Allele Identifier: CA375029336
Gene: SLC27A4 HGNC NCBI

Linked Data

gnomAD v4: 9-128345178-T-G
MyVariant Identifiers: chr9:g.131107457T>G (hg19) chr9:g.128345178T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128345178T>G , CM000671.2:g.128345178T>G GRCh38
NC_000009.11:g.131107457T>G , CM000671.1:g.131107457T>G GRCh37
NC_000009.10:g.130147278T>G NCBI36
NG_017057.1:g.9619T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000300456.5:c.185T>G MANE Select ENSP00000300456.3:p.Val62Gly
ENST00000300456.4:c.185T>G ENSP00000300456.3:p.Val62Gly
ENST00000372870.5:c.231+1897T>G ENSP00000361961.1:n.231+1897T>G
NM_005094.3:c.185T>G NP_005085.2:p.Val62Gly
XM_017014222.1:c.185T>G XP_016869711.1:p.Val62Gly
XM_024447391.1:c.185T>G XP_024303159.1:p.Val62Gly
NM_005094.4:c.185T>G MANE Select NP_005085.2:p.Val62Gly
Search 100 bp 5'
Search 100 bp 3'