Canonical Allele Identifier: CA1726792184
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404654A= , CM000669.2:g.94404654A= GRCh38
NC_000007.13:g.94033966A= , CM000669.1:g.94033966A= GRCh37
NC_000007.12:g.93871902A= NCBI36
NG_007405.1:g.15094A= , LRG_2:g.15094A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.325-39A= MANE Select ENSP00000297268.6:n.325-39A=
ENST00000297268.10:c.325-39A= ENSP00000297268.6:n.325-39A=
ENST00000620463.1:c.319-39A= ENSP00000477719.1:n.319-39A=
NM_000089.3:c.325-39A= , LRG_2t1:c.325-39A= NP_000080.2:n.325-39A=
NM_000089.4:c.325-39A= MANE Select NP_000080.2:n.325-39A=