Canonical Allele Identifier: CA2608926689

Gene: CXCL12

Linked Data

• gnomAD v4: 10-44370358-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44370358C>A , CM000672.2:g.44370358C>A	GRCh38
NC_000010.10:g.44865806C>A , CM000672.1:g.44865806C>A	GRCh37
NC_000010.9:g.44185812C>A	NCBI36
NG_016861.1:g.19740G>T
NG_016861.2:g.19740G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374429.6:c.*2970G>T	ENSP00000363551.2:n.*2970G>T
NM_000609.6:c.*2970G>T	NP_000600.1:n.*2970G>T
NM_001277990.1:c.*2530G>T	NP_001264919.1:n.*2530G>T
XR_001747171.1:n.331+8279G>T
XR_001747172.1:n.331+8279G>T
XR_001747173.1:n.331+8279G>T
XR_001747174.1:n.331+8279G>T
NM_000609.7:c.*2970G>T	NP_000600.1:n.*2970G>T
NM_001277990.2:c.*2530G>T	NP_001264919.1:n.*2530G>T