Canonical Allele Identifier: CA2347284311

Gene: SLC23A2

Linked Data

• dbSNP Id: rs2087654180

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.4977114C>T , CM000682.2:g.4977114C>T	GRCh38
NC_000020.10:g.4957760C>T , CM000682.1:g.4957760C>T	GRCh37
NC_000020.9:g.4905760C>T	NCBI36
NG_029959.1:g.29386G>A
NG_029959.2:g.38180G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338244.6:c.-281-6195G>A MANE Select	ENSP00000344322.1:n.-281-6195G>A
ENST00000338244.5:c.-281-6195G>A	ENSP00000344322.1:n.-281-6195G>A
ENST00000379333.5:c.-281-6195G>A	ENSP00000368637.1:n.-281-6195G>A
ENST00000468355.5:n.90-6199G>A
NM_005116.5:c.-281-6195G>A	NP_005107.4:n.-281-6195G>A
NM_203327.1:c.-281-6195G>A	NP_976072.1:n.-281-6195G>A
XM_011529414.1:c.-277-6199G>A	XP_011527716.1:n.-277-6199G>A
XM_011529417.1:c.-155+24292G>A	XP_011527719.1:n.-155+24292G>A
NM_005116.6:c.-281-6195G>A MANE Select	NP_005107.4:n.-281-6195G>A
NM_203327.2:c.-281-6195G>A	NP_976072.1:n.-281-6195G>A