Canonical Allele Identifier: CA730486923

Gene: SLC45A3

Linked Data

• dbSNP Id: rs1395845262
• MyVariant Identifiers: chr1:g.205638226G>C (hg19) ; chr1:g.205669098G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205669098G>C , CM000663.2:g.205669098G>C	GRCh38
NC_000001.10:g.205638226G>C , CM000663.1:g.205638226G>C	GRCh37
NC_000001.9:g.203904849G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000367145.4:c.-230-4212C>G MANE Select	ENSP00000356113.3:n.-230-4212C>G
ENST00000367145.3:c.-230-4212C>G	ENSP00000356113.3:n.-230-4212C>G
NM_033102.2:c.-230-4212C>G	NP_149093.1:n.-230-4212C>G
XM_005245556.2:c.-231+597C>G	XP_005245613.1:n.-231+597C>G
XM_005245557.3:c.-230-4212C>G	XP_005245614.1:n.-230-4212C>G
XM_005245559.3:c.-231+2852C>G	XP_005245616.1:n.-231+2852C>G
XM_005245560.2:c.-230-4212C>G	XP_005245617.1:n.-230-4212C>G
NM_033102.3:c.-230-4212C>G MANE Select	NP_149093.1:n.-230-4212C>G