Canonical Allele Identifier: CA1726793776
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94408221T= , CM000669.2:g.94408221T= GRCh38
NC_000007.13:g.94037533T= , CM000669.1:g.94037533T= GRCh37
NC_000007.12:g.93875469T= NCBI36
NG_007405.1:g.18661T= , LRG_2:g.18661T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.678T= MANE Select ENSP00000297268.6:p.Gly226=
ENST00000297268.10:c.678T= ENSP00000297268.6:p.Gly226=
ENST00000620463.1:c.672T= ENSP00000477719.1:p.Gly224=
NM_000089.3:c.678T= , LRG_2t1:c.678T= NP_000080.2:p.Gly226=
NM_000089.4:c.678T= MANE Select NP_000080.2:p.Gly226=