Canonical Allele Identifier: CA368220637
Gene: COL1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94409374G>C , CM000669.2:g.94409374G>C GRCh38
NC_000007.13:g.94038686G>C , CM000669.1:g.94038686G>C GRCh37
NC_000007.12:g.93876622G>C NCBI36
NG_007405.1:g.19814G>C , LRG_2:g.19814G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.845G>C MANE Select ENSP00000297268.6:p.Arg282Pro
ENST00000297268.10:c.845G>C ENSP00000297268.6:p.Arg282Pro
ENST00000620463.1:c.839G>C ENSP00000477719.1:p.Arg280Pro
NM_000089.3:c.845G>C , LRG_2t1:c.845G>C NP_000080.2:p.Arg282Pro
NM_000089.4:c.845G>C MANE Select NP_000080.2:p.Arg282Pro