Canonical Allele Identifier: CA206317054

Gene: CXCL12

Linked Data

• dbSNP Id: rs868724307
• MyVariant Identifiers: chr10:g.44865844C>T (hg19) ; chr10:g.44370396C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44370396C>T , CM000672.2:g.44370396C>T	GRCh38
NC_000010.10:g.44865844C>T , CM000672.1:g.44865844C>T	GRCh37
NC_000010.9:g.44185850C>T	NCBI36
NG_016861.1:g.19702G>A
NG_016861.2:g.19702G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374429.6:c.*2932G>A	ENSP00000363551.2:n.*2932G>A
NM_000609.6:c.*2932G>A	NP_000600.1:n.*2932G>A
NM_001277990.1:c.*2492G>A	NP_001264919.1:n.*2492G>A
XR_001747171.1:n.331+8241G>A
XR_001747172.1:n.331+8241G>A
XR_001747173.1:n.331+8241G>A
XR_001747174.1:n.331+8241G>A
NM_000609.7:c.*2932G>A	NP_000600.1:n.*2932G>A
NM_001277990.2:c.*2492G>A	NP_001264919.1:n.*2492G>A