Canonical Allele Identifier: CA1176673485
Gene: SLC44A5 HGNC NCBI

Linked Data

dbSNP Id: rs1676404124

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75641090T>C , CM000663.2:g.75641090T>C GRCh38
NC_000001.10:g.76106775T>C , CM000663.1:g.76106775T>C GRCh37
NC_000001.9:g.75879363T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011540981.1:c.-74+67935A>G XP_011539283.1:n.-74+67935A>G
XM_011540982.1:c.-74+1283A>G XP_011539284.1:n.-74+1283A>G
XM_011540984.1:c.-70+1283A>G XP_011539286.1:n.-70+1283A>G
XM_017000609.1:c.-70+1283A>G XP_016856098.1:n.-70+1283A>G
XM_017000610.1:c.-70+1283A>G XP_016856099.1:n.-70+1283A>G