Canonical Allele Identifier: CA2482673728
Gene: SLC45A3 HGNC NCBI

Linked Data

dbSNP Id: rs1671164342

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.205669101G>C , CM000663.2:g.205669101G>C GRCh38
NC_000001.10:g.205638229G>C , CM000663.1:g.205638229G>C GRCh37
NC_000001.9:g.203904852G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000367145.4:c.-230-4215C>G MANE Select ENSP00000356113.3:n.-230-4215C>G
ENST00000367145.3:c.-230-4215C>G ENSP00000356113.3:n.-230-4215C>G
NM_033102.2:c.-230-4215C>G NP_149093.1:n.-230-4215C>G
XM_005245556.2:c.-231+594C>G XP_005245613.1:n.-231+594C>G
XM_005245557.3:c.-230-4215C>G XP_005245614.1:n.-230-4215C>G
XM_005245559.3:c.-231+2849C>G XP_005245616.1:n.-231+2849C>G
XM_005245560.2:c.-230-4215C>G XP_005245617.1:n.-230-4215C>G
NM_033102.3:c.-230-4215C>G MANE Select NP_149093.1:n.-230-4215C>G