Canonical Allele Identifier: CA1160473269
Gene: CD164L2 HGNC NCBI

Linked Data

dbSNP Id: rs2016333084
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.27381397C>T , CM000663.2:g.27381397C>T GRCh38
NC_000001.10:g.27707887C>T , CM000663.1:g.27707887C>T GRCh37
NC_000001.9:g.27580474C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000374030.3:c.373+383G>A MANE Select ENSP00000363142.1:n.373+383G>A
ENST00000374027.7:c.373+383G>A ENSP00000363139.3:n.373+383G>A
ENST00000374030.2:c.373+383G>A ENSP00000363142.1:n.373+383G>A
NM_207397.3:c.373+383G>A NP_997280.2:n.373+383G>A
XM_005245868.3:c.373+383G>A XP_005245925.2:n.373+383G>A
XM_011541441.1:c.373+383G>A XP_011539743.1:n.373+383G>A
XR_241190.3:n.449+383G>A
NM_001330448.1:c.373+383G>A MANE Select NP_001317377.1:n.373+383G>A
NM_207397.4:c.373+383G>A NP_997280.2:n.373+383G>A
NM_207397.5:c.373+383G>A NP_997280.2:n.373+383G>A
Search 100 bp 5'
Search 100 bp 3'