Canonical Allele Identifier: CA927773100

Gene: CXCL12

Linked Data

• dbSNP Id: rs1839347559
• gnomAD v3: 10-44372826-G-A
• gnomAD v4: 10-44372826-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44372826G>A , CM000672.2:g.44372826G>A	GRCh38
NC_000010.10:g.44868274G>A , CM000672.1:g.44868274G>A	GRCh37
NC_000010.9:g.44188280G>A	NCBI36
NG_016861.1:g.17272C>T
NG_016861.2:g.17272C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000374429.6:c.*502C>T	ENSP00000363551.2:n.*502C>T
ENST00000395793.7:c.*62C>T	ENSP00000379139.3:n.*62C>T
NM_000609.6:c.*502C>T	NP_000600.1:n.*502C>T
NM_001277990.1:c.*62C>T	NP_001264919.1:n.*62C>T
XR_001747171.1:n.331+5811C>T
XR_001747172.1:n.331+5811C>T
XR_001747173.1:n.331+5811C>T
XR_001747174.1:n.331+5811C>T
NM_000609.7:c.*502C>T	NP_000600.1:n.*502C>T
NM_001277990.2:c.*62C>T	NP_001264919.1:n.*62C>T