Canonical Allele Identifier: CA359397920

Gene: SLC45A2

Linked Data

• dbSNP Id: rs1261044098
• gnomAD v2: 5-33984634-C-G
• gnomAD v4: 5-33984529-C-G
• MyVariant Identifiers: chr5:g.33984634C>G (hg19) ; chr5:g.33984529C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33984529C>G , CM000667.2:g.33984529C>G	GRCh38
NC_000005.9:g.33984634C>G , CM000667.1:g.33984634C>G	GRCh37
NC_000005.8:g.34020391C>G	NCBI36
NG_011691.2:g.5147G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.55G>C MANE Select	ENSP00000296589.4:p.Asp19His
ENST00000296589.8:c.55G>C	ENSP00000296589.4:p.Asp19His
ENST00000382102.7:c.55G>C	ENSP00000371534.3:p.Asp19His
ENST00000505056.1:n.34G>C
ENST00000509381.1:c.55G>C	ENSP00000421100.1:p.Asp19His
NM_001012509.3:c.55G>C	NP_001012527.1:p.Asp19His
NM_001297417.2:c.55G>C	NP_001284346.2:p.Asp19His
NM_016180.4:c.55G>C	NP_057264.3:p.Asp19His
XM_011514052.1:c.55G>C	XP_011512354.1:p.Asp19His
XR_925620.1:n.616G>C
NM_016180.5:c.55G>C MANE Select	NP_057264.4:p.Asp19His
NM_001012509.4:c.55G>C	NP_001012527.2:p.Asp19His
NM_001297417.3:c.55G>C	NP_001284346.2:p.Asp19His
NM_001297417.4:c.55G>C	NP_001284346.2:p.Asp19His