Canonical Allele Identifier: CA2608926779

Gene: CXCL12

Linked Data

• gnomAD v4: 10-44370538-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44370538G>T , CM000672.2:g.44370538G>T	GRCh38
NC_000010.10:g.44865986G>T , CM000672.1:g.44865986G>T	GRCh37
NC_000010.9:g.44185992G>T	NCBI36
NG_016861.1:g.19560C>A
NG_016861.2:g.19560C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374429.6:c.*2790C>A	ENSP00000363551.2:n.*2790C>A
NM_000609.6:c.*2790C>A	NP_000600.1:n.*2790C>A
NM_001277990.1:c.*2350C>A	NP_001264919.1:n.*2350C>A
XR_001747171.1:n.331+8099C>A
XR_001747172.1:n.331+8099C>A
XR_001747173.1:n.331+8099C>A
XR_001747174.1:n.331+8099C>A
NM_000609.7:c.*2790C>A	NP_000600.1:n.*2790C>A
NM_001277990.2:c.*2350C>A	NP_001264919.1:n.*2350C>A