Canonical Allele Identifier: CA927778398

Gene: CXCL12

Linked Data

• dbSNP Id: rs1839810325
• gnomAD v3: 10-44386012-C-T
• gnomAD v4: 10-44386012-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44386012C>T , CM000672.2:g.44386012C>T	GRCh38
NC_000010.10:g.44881460C>T , CM000672.1:g.44881460C>T	GRCh37
NC_000010.9:g.44201466C>T	NCBI36
NG_016861.1:g.4086G>A
NG_016861.2:g.4086G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496375.1:n.482G>A