Canonical Allele Identifier: CA679128550

Gene: SLC22A24

Linked Data

• dbSNP Id: rs1431231588
• gnomAD v3: 11-63137286-G-C
• gnomAD v4: 11-63137286-G-C
• MyVariant Identifiers: chr11:g.62904758G>C (hg19) ; chr11:g.63137286G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.63137286G>C , CM000673.2:g.63137286G>C	GRCh38
NC_000011.9:g.62904758G>C , CM000673.1:g.62904758G>C	GRCh37
NC_000011.8:g.62661334G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326192.5:c.403-2518C>G	ENSP00000321549.5:n.403-2518C>G
ENST00000417740.5:c.403-2518C>G	ENSP00000396586.1:n.403-2518C>G
ENST00000612278.4:c.403-2518C>G MANE Select	ENSP00000480336.1:n.403-2518C>G
NM_001136506.2:c.403-2518C>G MANE Select	NP_001129978.2:n.403-2518C>G
NM_173586.2:c.403-2518C>G	NP_775857.2:n.403-2518C>G
XM_011544964.1:c.403-2518C>G	XP_011543266.1:n.403-2518C>G
XM_011544965.1:c.403-2518C>G	XP_011543267.1:n.403-2518C>G
XM_011544966.1:c.403-2518C>G	XP_011543268.1:n.403-2518C>G
XM_011544967.1:c.403-2518C>G	XP_011543269.1:n.403-2518C>G
NM_173586.3:c.403-2518C>G	NP_775857.2:n.403-2518C>G