Canonical Allele Identifier: CA1726781676
Gene: COL1A2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94425664G= , CM000669.2:g.94425664G= GRCh38
NC_000007.13:g.94054976G= , CM000669.1:g.94054976G= GRCh37
NC_000007.12:g.93892912G= NCBI36
NG_007405.1:g.36104G= , LRG_2:g.36104G=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2835+1G= MANE Select ENSP00000297268.6:n.2835+1G=
ENST00000297268.10:c.2835+1G= ENSP00000297268.6:n.2835+1G=
ENST00000469732.1:n.618+1G=
ENST00000478215.1:n.394+1G=
ENST00000481570.5:n.2808+1G=
ENST00000620463.1:c.2829+1G= ENSP00000477719.1:n.2829+1G=
NM_000089.3:c.2835+1G= , LRG_2t1:c.2835+1G= NP_000080.2:n.2835+1G=
NM_000089.4:c.2835+1G= MANE Select NP_000080.2:n.2835+1G=
Search 100 bp 5'
Search 100 bp 3'