Canonical Allele Identifier: CA2608929344
Gene: CXCL12 HGNC NCBI

Linked Data

gnomAD v4: 10-44372825-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.44372825G>C , CM000672.2:g.44372825G>C GRCh38
NC_000010.10:g.44868273G>C , CM000672.1:g.44868273G>C GRCh37
NC_000010.9:g.44188279G>C NCBI36
NG_016861.1:g.17273C>G
NG_016861.2:g.17273C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000374429.6:c.*503C>G ENSP00000363551.2:n.*503C>G
ENST00000395793.7:c.*63C>G ENSP00000379139.3:n.*63C>G
NM_000609.6:c.*503C>G NP_000600.1:n.*503C>G
NM_001277990.1:c.*63C>G NP_001264919.1:n.*63C>G
XR_001747171.1:n.331+5812C>G
XR_001747172.1:n.331+5812C>G
XR_001747173.1:n.331+5812C>G
XR_001747174.1:n.331+5812C>G
NM_000609.7:c.*503C>G NP_000600.1:n.*503C>G
NM_001277990.2:c.*63C>G NP_001264919.1:n.*63C>G
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