Canonical Allele Identifier: CA810006501

Gene: SLC45A2

Linked Data

• dbSNP Id: rs1487286416
• gnomAD v3: 5-33951366-C-T
• gnomAD v4: 5-33951366-C-T
• MyVariant Identifiers: chr5:g.33951471C>T (hg19) ; chr5:g.33951366C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33951366C>T , CM000667.2:g.33951366C>T	GRCh38
NC_000005.9:g.33951471C>T , CM000667.1:g.33951471C>T	GRCh37
NC_000005.8:g.33987228C>T	NCBI36
NG_011691.2:g.38310G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.1156+188G>A MANE Select	ENSP00000296589.4:n.1156+188G>A
ENST00000296589.8:c.1156+188G>A	ENSP00000296589.4:n.1156+188G>A
ENST00000382102.7:c.1156+188G>A	ENSP00000371534.3:n.1156+188G>A
ENST00000510600.1:c.631+188G>A	ENSP00000424010.1:n.631+188G>A
NM_001012509.3:c.1156+188G>A	NP_001012527.1:n.1156+188G>A
NM_016180.4:c.1156+188G>A	NP_057264.3:n.1156+188G>A
XM_011514051.1:c.754+188G>A	XP_011512353.1:n.754+188G>A
XR_925620.1:n.1973+188G>A
NM_016180.5:c.1156+188G>A MANE Select	NP_057264.4:n.1156+188G>A
NM_001012509.4:c.1156+188G>A	NP_001012527.2:n.1156+188G>A