Canonical Allele Identifier: CA2683772090
Gene: COL1A2 HGNC NCBI

Linked Data

gnomAD v4: 7-94422888-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94422888T>A , CM000669.2:g.94422888T>A GRCh38
NC_000007.13:g.94052200T>A , CM000669.1:g.94052200T>A GRCh37
NC_000007.12:g.93890136T>A NCBI36
NG_007405.1:g.33328T>A , LRG_2:g.33328T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2404-69T>A MANE Select ENSP00000297268.6:n.2404-69T>A
ENST00000297268.10:c.2404-69T>A ENSP00000297268.6:n.2404-69T>A
ENST00000481570.5:n.418T>A
ENST00000497316.5:n.801-69T>A
ENST00000620463.1:c.2398-69T>A ENSP00000477719.1:n.2398-69T>A
NM_000089.3:c.2404-69T>A , LRG_2t1:c.2404-69T>A NP_000080.2:n.2404-69T>A
NM_000089.4:c.2404-69T>A MANE Select NP_000080.2:n.2404-69T>A