Canonical Allele Identifier: CA927778438

Gene: CXCL12

Linked Data

• dbSNP Id: rs1839812808
• gnomAD v3: 10-44386092-C-T
• gnomAD v4: 10-44386092-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44386092C>T , CM000672.2:g.44386092C>T	GRCh38
NC_000010.10:g.44881540C>T , CM000672.1:g.44881540C>T	GRCh37
NC_000010.9:g.44201546C>T	NCBI36
NG_016861.1:g.4006G>A
NG_016861.2:g.4006G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496375.1:n.402G>A