Canonical Allele Identifier: CA2175373478
Gene: SLC24A5 HGNC NCBI

Linked Data

dbSNP Id: rs1420214639
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48134195T>A , CM000677.2:g.48134195T>A GRCh38
NC_000015.9:g.48426392T>A , CM000677.1:g.48426392T>A GRCh37
NC_000015.8:g.46213684T>A NCBI36
NG_011500.1:g.18224T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000341459.8:c.302-63T>A MANE Select ENSP00000341550.3:n.302-63T>A
ENST00000341459.7:c.302-63T>A ENSP00000341550.3:n.302-63T>A
ENST00000449382.2:c.122-63T>A ENSP00000389966.2:n.122-63T>A
ENST00000463289.1:n.62-63T>A
NM_205850.2:c.302-63T>A NP_995322.1:n.302-63T>A
XM_011521458.1:c.302-63T>A XP_011519760.1:n.302-63T>A
XM_017022079.1:c.-38-63T>A XP_016877568.1:n.-38-63T>A
XM_017022080.1:c.-38-63T>A XP_016877569.1:n.-38-63T>A
XM_024449901.1:c.-38-63T>A XP_024305669.1:n.-38-63T>A
NM_205850.3:c.302-63T>A MANE Select NP_995322.1:n.302-63T>A
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