Canonical Allele Identifier: CA1726792152
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404585T= , CM000669.2:g.94404585T= GRCh38
NC_000007.13:g.94033897T= , CM000669.1:g.94033897T= GRCh37
NC_000007.12:g.93871833T= NCBI36
NG_007405.1:g.15025T= , LRG_2:g.15025T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.309T= MANE Select ENSP00000297268.6:p.Gly103=
ENST00000297268.10:c.309T= ENSP00000297268.6:p.Gly103=
ENST00000620463.1:c.303T= ENSP00000477719.1:p.Gly101=
NM_000089.3:c.309T= , LRG_2t1:c.309T= NP_000080.2:p.Gly103=
NM_000089.4:c.309T= MANE Select NP_000080.2:p.Gly103=