Canonical Allele Identifier: CA368220645
Gene: COL1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94409379G>T , CM000669.2:g.94409379G>T GRCh38
NC_000007.13:g.94038691G>T , CM000669.1:g.94038691G>T GRCh37
NC_000007.12:g.93876627G>T NCBI36
NG_007405.1:g.19819G>T , LRG_2:g.19819G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.850G>T MANE Select ENSP00000297268.6:p.Glu284Ter
ENST00000297268.10:c.850G>T ENSP00000297268.6:p.Glu284Ter
ENST00000620463.1:c.844G>T ENSP00000477719.1:p.Glu282Ter
NM_000089.3:c.850G>T , LRG_2t1:c.850G>T NP_000080.2:p.Glu284Ter
NM_000089.4:c.850G>T MANE Select NP_000080.2:p.Glu284Ter