Canonical Allele Identifier: CA206317061

Gene: CXCL12

Linked Data

• dbSNP Id: rs978164872
• MyVariant Identifiers: chr10:g.44865859G>A (hg19) ; chr10:g.44370411G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44370411G>A , CM000672.2:g.44370411G>A	GRCh38
NC_000010.10:g.44865859G>A , CM000672.1:g.44865859G>A	GRCh37
NC_000010.9:g.44185865G>A	NCBI36
NG_016861.1:g.19687C>T
NG_016861.2:g.19687C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374429.6:c.*2917C>T	ENSP00000363551.2:n.*2917C>T
NM_000609.6:c.*2917C>T	NP_000600.1:n.*2917C>T
NM_001277990.1:c.*2477C>T	NP_001264919.1:n.*2477C>T
XR_001747171.1:n.331+8226C>T
XR_001747172.1:n.331+8226C>T
XR_001747173.1:n.331+8226C>T
XR_001747174.1:n.331+8226C>T
NM_000609.7:c.*2917C>T	NP_000600.1:n.*2917C>T
NM_001277990.2:c.*2477C>T	NP_001264919.1:n.*2477C>T