Canonical Allele Identifier: CA1978109533

Gene: SLC22A24

Linked Data

• dbSNP Id: rs2087383060

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.63137384A>G , CM000673.2:g.63137384A>G	GRCh38
NC_000011.9:g.62904856A>G , CM000673.1:g.62904856A>G	GRCh37
NC_000011.8:g.62661432A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000326192.5:c.403-2616T>C	ENSP00000321549.5:n.403-2616T>C
ENST00000417740.5:c.403-2616T>C	ENSP00000396586.1:n.403-2616T>C
ENST00000612278.4:c.403-2616T>C MANE Select	ENSP00000480336.1:n.403-2616T>C
NM_001136506.2:c.403-2616T>C MANE Select	NP_001129978.2:n.403-2616T>C
NM_173586.2:c.403-2616T>C	NP_775857.2:n.403-2616T>C
XM_011544964.1:c.403-2616T>C	XP_011543266.1:n.403-2616T>C
XM_011544965.1:c.403-2616T>C	XP_011543267.1:n.403-2616T>C
XM_011544966.1:c.403-2616T>C	XP_011543268.1:n.403-2616T>C
XM_011544967.1:c.403-2616T>C	XP_011543269.1:n.403-2616T>C
NM_173586.3:c.403-2616T>C	NP_775857.2:n.403-2616T>C