Canonical Allele Identifier: CA1726790834
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94401445C= , CM000669.2:g.94401445C= GRCh38
NC_000007.13:g.94030757C= , CM000669.1:g.94030757C= GRCh37
NC_000007.12:g.93868693C= NCBI36
NG_007405.1:g.11885C= , LRG_2:g.11885C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.226-122C= MANE Select ENSP00000297268.6:n.226-122C=
ENST00000297268.10:c.226-122C= ENSP00000297268.6:n.226-122C=
ENST00000620463.1:c.220-122C= ENSP00000477719.1:n.220-122C=
NM_000089.3:c.226-122C= , LRG_2t1:c.226-122C= NP_000080.2:n.226-122C=
NM_000089.4:c.226-122C= MANE Select NP_000080.2:n.226-122C=