Canonical Allele Identifier: CA2608929334
Gene: CXCL12 HGNC NCBI

Linked Data

gnomAD v4: 10-44372814-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44372814C>T , CM000672.2:g.44372814C>T GRCh38
NC_000010.10:g.44868262C>T , CM000672.1:g.44868262C>T GRCh37
NC_000010.9:g.44188268C>T NCBI36
NG_016861.1:g.17284G>A
NG_016861.2:g.17284G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374429.6:c.*514G>A ENSP00000363551.2:n.*514G>A
ENST00000395793.7:c.*74G>A ENSP00000379139.3:n.*74G>A
NM_000609.6:c.*514G>A NP_000600.1:n.*514G>A
NM_001277990.1:c.*74G>A NP_001264919.1:n.*74G>A
XR_001747171.1:n.331+5823G>A
XR_001747172.1:n.331+5823G>A
XR_001747173.1:n.331+5823G>A
XR_001747174.1:n.331+5823G>A
NM_000609.7:c.*514G>A NP_000600.1:n.*514G>A
NM_001277990.2:c.*74G>A NP_001264919.1:n.*74G>A
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