Canonical Allele Identifier: CA368224152
Gene: COL1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94423108C>A , CM000669.2:g.94423108C>A GRCh38
NC_000007.13:g.94052420C>A , CM000669.1:g.94052420C>A GRCh37
NC_000007.12:g.93890356C>A NCBI36
NG_007405.1:g.33548C>A , LRG_2:g.33548C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.2555C>A MANE Select ENSP00000297268.6:p.Ala852Asp
ENST00000297268.10:c.2555C>A ENSP00000297268.6:p.Ala852Asp
ENST00000481570.5:n.638C>A
ENST00000497316.5:n.952C>A
ENST00000620463.1:c.2549C>A ENSP00000477719.1:p.Ala850Asp
NM_000089.3:c.2555C>A , LRG_2t1:c.2555C>A NP_000080.2:p.Ala852Asp
NM_000089.4:c.2555C>A MANE Select NP_000080.2:p.Ala852Asp