Canonical Allele Identifier: CA443658878
Gene: SLC45A2 HGNC NCBI

Linked Data

gnomAD v4: 5-33944801-T-A
MyVariant Identifiers: chr5:g.33944906T>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33944801T>A , CM000667.2:g.33944801T>A GRCh38
NC_000005.9:g.33944906T>A , CM000667.1:g.33944906T>A GRCh37
NC_000005.8:g.33980663T>A NCBI36
NG_011691.2:g.44875A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.1440A>T MANE Select ENSP00000296589.4:p.Thr480=
ENST00000296589.8:c.1440A>T ENSP00000296589.4:p.Thr480=
NM_016180.4:c.1440A>T NP_057264.3:p.Thr480=
XM_011514051.1:c.1038A>T XP_011512353.1:p.Thr346=
NM_016180.5:c.1440A>T MANE Select NP_057264.4:p.Thr480=
Search 100 bp 5'
Search 100 bp 3'