Canonical Allele Identifier: CA2608926699

Gene: CXCL12

Linked Data

• gnomAD v4: 10-44370375-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44370375C>A , CM000672.2:g.44370375C>A	GRCh38
NC_000010.10:g.44865823C>A , CM000672.1:g.44865823C>A	GRCh37
NC_000010.9:g.44185829C>A	NCBI36
NG_016861.1:g.19723G>T
NG_016861.2:g.19723G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374429.6:c.*2953G>T	ENSP00000363551.2:n.*2953G>T
NM_000609.6:c.*2953G>T	NP_000600.1:n.*2953G>T
NM_001277990.1:c.*2513G>T	NP_001264919.1:n.*2513G>T
XR_001747171.1:n.331+8262G>T
XR_001747172.1:n.331+8262G>T
XR_001747173.1:n.331+8262G>T
XR_001747174.1:n.331+8262G>T
NM_000609.7:c.*2953G>T	NP_000600.1:n.*2953G>T
NM_001277990.2:c.*2513G>T	NP_001264919.1:n.*2513G>T