Canonical Allele Identifier: CA14865039
Gene: SLC19A1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1023159

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45546266G>A , CM000683.2:g.45546266G>A GRCh38
NC_000021.8:g.46966180G>A , CM000683.1:g.46966180G>A GRCh37
NC_000021.7:g.45790608G>A NCBI36
NG_028278.1:g.1206C>T
NG_028278.2:g.21878C>T

Transcript Alleles

HGVS Amino-acid change
XM_011529697.1:c.-125-1641C>T XP_011527999.1:p.=
XM_011529700.1:c.-49-8258C>T XP_011528002.1:p.=
XM_011529705.1:c.-137-1629C>T XP_011528007.1:p.=
XM_011529707.1:c.-137-1629C>T XP_011528009.1:p.=
XM_011529709.1:c.-407-8258C>T XP_011528011.1:p.=
XM_011529710.1:c.-165-14118C>T XP_011528012.1:p.=
NM_001352511.1:c.-49-8258C>T VV NP_001339440.1:p.=
XM_011529700.2:c.-49-8258C>T
XM_011529709.2:c.-407-8258C>T