Canonical Allele Identifier: CA430503059
Gene: SLC40A1 HGNC NCBI

Linked Data

dbSNP Id: rs2030845619
MyVariant Identifiers: chr2:g.190428728G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189564002G>A , CM000664.2:g.189564002G>A GRCh38
NC_000002.11:g.190428728G>A , CM000664.1:g.190428728G>A GRCh37
NC_000002.10:g.190136973G>A NCBI36
NG_009027.1:g.21810C>T , LRG_837:g.21810C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261024.7:c.984C>T MANE Select ENSP00000261024.3:p.Thr328=
ENST00000261024.6:c.984C>T ENSP00000261024.2:p.Thr328=
NM_014585.5:c.984C>T , LRG_837t1:c.984C>T NP_055400.1:p.Thr328=
XM_005246505.1:c.864C>T XP_005246562.1:p.Thr288=
XM_005246505.2:c.864C>T XP_005246562.1:p.Thr288=
XM_017003938.2:c.864C>T XP_016859427.1:p.Thr288=
NM_014585.6:c.984C>T MANE Select NP_055400.1:p.Thr328=