Canonical Allele Identifier: CA665400773

Gene: CXCL12

Linked Data

• dbSNP Id: rs1222297711
• gnomAD v3: 10-44370476-G-T
• gnomAD v4: 10-44370476-G-T
• MyVariant Identifiers: chr10:g.44865924G>T (hg19) ; chr10:g.44370476G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44370476G>T , CM000672.2:g.44370476G>T	GRCh38
NC_000010.10:g.44865924G>T , CM000672.1:g.44865924G>T	GRCh37
NC_000010.9:g.44185930G>T	NCBI36
NG_016861.1:g.19622C>A
NG_016861.2:g.19622C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000374429.6:c.*2852C>A	ENSP00000363551.2:n.*2852C>A
NM_000609.6:c.*2852C>A	NP_000600.1:n.*2852C>A
NM_001277990.1:c.*2412C>A	NP_001264919.1:n.*2412C>A
XR_001747171.1:n.331+8161C>A
XR_001747172.1:n.331+8161C>A
XR_001747173.1:n.331+8161C>A
XR_001747174.1:n.331+8161C>A
NM_000609.7:c.*2852C>A	NP_000600.1:n.*2852C>A
NM_001277990.2:c.*2412C>A	NP_001264919.1:n.*2412C>A