Canonical Allele Identifier: CA1906433332

Gene: CXCL12

Genomic Alleles

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

Transcript Alleles

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