Canonical Allele Identifier: CA467482892
Gene: SLC27A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.131107446C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128345167C>G , CM000671.2:g.128345167C>G GRCh38
NC_000009.11:g.131107446C>G , CM000671.1:g.131107446C>G GRCh37
NC_000009.10:g.130147267C>G NCBI36
NG_017057.1:g.9608C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000300456.5:c.174C>G MANE Select ENSP00000300456.3:p.Val58=
ENST00000300456.4:c.174C>G ENSP00000300456.3:p.Val58=
ENST00000372870.5:c.231+1886C>G ENSP00000361961.1:n.231+1886C>G
NM_005094.3:c.174C>G NP_005085.2:p.Val58=
XM_017014222.1:c.174C>G XP_016869711.1:p.Val58=
XM_024447391.1:c.174C>G XP_024303159.1:p.Val58=
NM_005094.4:c.174C>G MANE Select NP_005085.2:p.Val58=
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