Canonical Allele Identifier: CA2175373439
Gene: SLC24A5 HGNC NCBI

Linked Data

dbSNP Id: rs2038836706

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48134151A>C , CM000677.2:g.48134151A>C GRCh38
NC_000015.9:g.48426348A>C , CM000677.1:g.48426348A>C GRCh37
NC_000015.8:g.46213640A>C NCBI36
NG_011500.1:g.18180A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000341459.8:c.302-107A>C MANE Select ENSP00000341550.3:n.302-107A>C
ENST00000341459.7:c.302-107A>C ENSP00000341550.3:n.302-107A>C
ENST00000449382.2:c.122-107A>C ENSP00000389966.2:n.122-107A>C
ENST00000463289.1:n.62-107A>C
NM_205850.2:c.302-107A>C NP_995322.1:n.302-107A>C
XM_011521458.1:c.302-107A>C XP_011519760.1:n.302-107A>C
XM_017022079.1:c.-38-107A>C XP_016877568.1:n.-38-107A>C
XM_017022080.1:c.-38-107A>C XP_016877569.1:n.-38-107A>C
XM_024449901.1:c.-38-107A>C XP_024305669.1:n.-38-107A>C
NM_205850.3:c.302-107A>C MANE Select NP_995322.1:n.302-107A>C