Canonical Allele Identifier: CA1726763272
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94415191A= , CM000669.2:g.94415191A= GRCh38
NC_000007.13:g.94044503A= , CM000669.1:g.94044503A= GRCh37
NC_000007.12:g.93882439A= NCBI36
NG_007405.1:g.25631A= , LRG_2:g.25631A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.1720-35A= MANE Select ENSP00000297268.6:n.1720-35A=
ENST00000297268.10:c.1720-35A= ENSP00000297268.6:n.1720-35A=
ENST00000473573.5:n.57-35A=
ENST00000488298.5:n.144-35A=
ENST00000620463.1:c.1714-35A= ENSP00000477719.1:n.1714-35A=
NM_000089.3:c.1720-35A= , LRG_2t1:c.1720-35A= NP_000080.2:n.1720-35A=
NM_000089.4:c.1720-35A= MANE Select NP_000080.2:n.1720-35A=