Canonical Allele Identifier: CA651752735
Gene: COL1A2 HGNC NCBI

Linked Data

COSMIC: COSN8047857
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404775A>G , CM000669.2:g.94404775A>G GRCh38
NC_000007.13:g.94034087A>G , CM000669.1:g.94034087A>G GRCh37
NC_000007.12:g.93872023A>G NCBI36
NG_007405.1:g.15215A>G , LRG_2:g.15215A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.378+29A>G MANE Select ENSP00000297268.6:n.378+29A>G
ENST00000297268.10:c.378+29A>G ENSP00000297268.6:n.378+29A>G
ENST00000620463.1:c.372+29A>G ENSP00000477719.1:n.372+29A>G
NM_000089.3:c.378+29A>G , LRG_2t1:c.378+29A>G NP_000080.2:n.378+29A>G
NM_000089.4:c.378+29A>G MANE Select NP_000080.2:n.378+29A>G
Search 100 bp 5'
Search 100 bp 3'