Canonical Allele Identifier: CA368220287
Gene: COL1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94408217T>A , CM000669.2:g.94408217T>A GRCh38
NC_000007.13:g.94037529T>A , CM000669.1:g.94037529T>A GRCh37
NC_000007.12:g.93875465T>A NCBI36
NG_007405.1:g.18657T>A , LRG_2:g.18657T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.674T>A MANE Select ENSP00000297268.6:p.Val225Asp
ENST00000297268.10:c.674T>A ENSP00000297268.6:p.Val225Asp
ENST00000620463.1:c.668T>A ENSP00000477719.1:p.Val223Asp
NM_000089.3:c.674T>A , LRG_2t1:c.674T>A NP_000080.2:p.Val225Asp
NM_000089.4:c.674T>A MANE Select NP_000080.2:p.Val225Asp