Canonical Allele Identifier: CA665400746

Gene: CXCL12

Linked Data

• dbSNP Id: rs1248634939
• gnomAD v3: 10-44370463-G-GGTCT
• gnomAD v4: 10-44370463-G-GGTCT
• MyVariant Identifiers: chr10:g.44865911_44865912insGTCT (hg19) ; chr10:g.44370463_44370464insGTCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44370465_44370468dup , CM000672.2:g.44370465_44370468dup	GRCh38
NC_000010.10:g.44865913_44865916dup , CM000672.1:g.44865913_44865916dup	GRCh37
NC_000010.9:g.44185919_44185922dup	NCBI36
NG_016861.1:g.19631_19634dup
NG_016861.2:g.19631_19634dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374429.6:c.*2861_*2864dup	ENSP00000363551.2:n.*2861_*2864dup
NM_000609.6:c.*2861_*2864dup	NP_000600.1:n.*2861_*2864dup
NM_001277990.1:c.*2421_*2424dup	NP_001264919.1:n.*2421_*2424dup
XR_001747171.1:n.331+8170_331+8173dup
XR_001747172.1:n.331+8170_331+8173dup
XR_001747173.1:n.331+8170_331+8173dup
XR_001747174.1:n.331+8170_331+8173dup
NM_000609.7:c.*2861_*2864dup	NP_000600.1:n.*2861_*2864dup
NM_001277990.2:c.*2421_*2424dup	NP_001264919.1:n.*2421_*2424dup