Canonical Allele Identifier: CA1538211575
Gene: SLC45A2 HGNC NCBI

Linked Data

dbSNP Id: rs1752088938

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33951353G>A , CM000667.2:g.33951353G>A GRCh38
NC_000005.9:g.33951458G>A , CM000667.1:g.33951458G>A GRCh37
NC_000005.8:g.33987215G>A NCBI36
NG_011691.2:g.38323C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.1156+201C>T MANE Select ENSP00000296589.4:n.1156+201C>T
ENST00000296589.8:c.1156+201C>T ENSP00000296589.4:n.1156+201C>T
ENST00000382102.7:c.1156+201C>T ENSP00000371534.3:n.1156+201C>T
ENST00000510600.1:c.631+201C>T ENSP00000424010.1:n.631+201C>T
NM_001012509.3:c.1156+201C>T NP_001012527.1:n.1156+201C>T
NM_016180.4:c.1156+201C>T NP_057264.3:n.1156+201C>T
XM_011514051.1:c.754+201C>T XP_011512353.1:n.754+201C>T
XR_925620.1:n.1973+201C>T
NM_016180.5:c.1156+201C>T MANE Select NP_057264.4:n.1156+201C>T
NM_001012509.4:c.1156+201C>T NP_001012527.2:n.1156+201C>T