Canonical Allele Identifier: CA359390206

Gene: SLC45A2

Linked Data

• dbSNP Id: rs1310846892
• gnomAD v3: 5-33951675-A-G
• gnomAD v4: 5-33951675-A-G
• MyVariant Identifiers: chr5:g.33951780A>G (hg19) ; chr5:g.33951675A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33951675A>G , CM000667.2:g.33951675A>G	GRCh38
NC_000005.9:g.33951780A>G , CM000667.1:g.33951780A>G	GRCh37
NC_000005.8:g.33987537A>G	NCBI36
NG_011691.2:g.38001T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.1035T>C MANE Select	ENSP00000296589.4:p.Ile345=
ENST00000296589.8:c.1035T>C	ENSP00000296589.4:p.Ile345=
ENST00000382102.7:c.1035T>C	ENSP00000371534.3:p.Ile345=
ENST00000509381.1:c.709T>C	ENSP00000421100.1:p.Cys237Arg
ENST00000510600.1:c.510T>C	ENSP00000424010.1:p.Ile170=
NM_001012509.3:c.1035T>C	NP_001012527.1:p.Ile345=
NM_001297417.2:c.709T>C	NP_001284346.2:p.Cys237Arg
NM_016180.4:c.1035T>C	NP_057264.3:p.Ile345=
XM_011514051.1:c.633T>C	XP_011512353.1:p.Ile211=
XR_925620.1:n.1852T>C
NM_016180.5:c.1035T>C MANE Select	NP_057264.4:p.Ile345=
NM_001012509.4:c.1035T>C	NP_001012527.2:p.Ile345=
NM_001297417.3:c.709T>C	NP_001284346.2:p.Cys237Arg
NM_001297417.4:c.709T>C	NP_001284346.2:p.Cys237Arg