Canonical Allele Identifier: CA1726792262
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404862A= , CM000669.2:g.94404862A= GRCh38
NC_000007.13:g.94034174A= , CM000669.1:g.94034174A= GRCh37
NC_000007.12:g.93872110A= NCBI36
NG_007405.1:g.15302A= , LRG_2:g.15302A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.402A= MANE Select ENSP00000297268.6:p.Pro134=
ENST00000297268.10:c.402A= ENSP00000297268.6:p.Pro134=
ENST00000620463.1:c.396A= ENSP00000477719.1:p.Pro132=
NM_000089.3:c.402A= , LRG_2t1:c.402A= NP_000080.2:p.Pro134=
NM_000089.4:c.402A= MANE Select NP_000080.2:p.Pro134=