Canonical Allele Identifier: CA679128601
Gene: SLC22A24 HGNC NCBI

Linked Data

dbSNP Id: rs1388993865
MyVariant Identifiers: chr11:g.62904970G>T (hg19) chr11:g.63137498G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.63137498G>T , CM000673.2:g.63137498G>T GRCh38
NC_000011.9:g.62904970G>T , CM000673.1:g.62904970G>T GRCh37
NC_000011.8:g.62661546G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326192.5:c.403-2730C>A ENSP00000321549.5:n.403-2730C>A
ENST00000417740.5:c.403-2730C>A ENSP00000396586.1:n.403-2730C>A
ENST00000612278.4:c.403-2730C>A MANE Select ENSP00000480336.1:n.403-2730C>A
NM_001136506.2:c.403-2730C>A MANE Select NP_001129978.2:n.403-2730C>A
NM_173586.2:c.403-2730C>A NP_775857.2:n.403-2730C>A
XM_011544964.1:c.403-2730C>A XP_011543266.1:n.403-2730C>A
XM_011544965.1:c.403-2730C>A XP_011543267.1:n.403-2730C>A
XM_011544966.1:c.403-2730C>A XP_011543268.1:n.403-2730C>A
XM_011544967.1:c.403-2730C>A XP_011543269.1:n.403-2730C>A
NM_173586.3:c.403-2730C>A NP_775857.2:n.403-2730C>A
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