Canonical Allele Identifier: CA665400712
Gene: CXCL12 HGNC NCBI

Linked Data

dbSNP Id: rs1804429
MyVariant Identifiers: chr10:g.44865841A>T (hg19) chr10:g.44370393A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44370393A>T , CM000672.2:g.44370393A>T GRCh38
NC_000010.10:g.44865841A>T , CM000672.1:g.44865841A>T GRCh37
NC_000010.9:g.44185847A>T NCBI36
NG_016861.1:g.19705T>A
NG_016861.2:g.19705T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374429.6:c.*2935T>A ENSP00000363551.2:n.*2935T>A
NM_000609.6:c.*2935T>A NP_000600.1:n.*2935T>A
NM_001277990.1:c.*2495T>A NP_001264919.1:n.*2495T>A
XR_001747171.1:n.331+8244T>A
XR_001747172.1:n.331+8244T>A
XR_001747173.1:n.331+8244T>A
XR_001747174.1:n.331+8244T>A
NM_000609.7:c.*2935T>A NP_000600.1:n.*2935T>A
NM_001277990.2:c.*2495T>A NP_001264919.1:n.*2495T>A
Search 100 bp 5'
Search 100 bp 3'