Canonical Allele Identifier: CA368224079
Gene: COL1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94423071C>T , CM000669.2:g.94423071C>T GRCh38
NC_000007.13:g.94052383C>T , CM000669.1:g.94052383C>T GRCh37
NC_000007.12:g.93890319C>T NCBI36
NG_007405.1:g.33511C>T , LRG_2:g.33511C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2518C>T MANE Select ENSP00000297268.6:p.Pro840Ser
ENST00000297268.10:c.2518C>T ENSP00000297268.6:p.Pro840Ser
ENST00000481570.5:n.601C>T
ENST00000497316.5:n.915C>T
ENST00000620463.1:c.2512C>T ENSP00000477719.1:p.Pro838Ser
NM_000089.3:c.2518C>T , LRG_2t1:c.2518C>T NP_000080.2:p.Pro840Ser
NM_000089.4:c.2518C>T MANE Select NP_000080.2:p.Pro840Ser