Canonical Allele Identifier: CA162919400
Gene: COL1A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1194111
ClinVar RCV Id: RCV001556728
dbSNP Id: rs41316926
gnomAD v2: 7-94038508-C-T
gnomAD v3: 7-94409196-C-T
gnomAD v4: 7-94409196-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94409196C>T , CM000669.2:g.94409196C>T GRCh38
NC_000007.13:g.94038508C>T , CM000669.1:g.94038508C>T GRCh37
NC_000007.12:g.93876444C>T NCBI36
NG_007405.1:g.19636C>T , LRG_2:g.19636C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.793-126C>T MANE Select ENSP00000297268.6:n.793-126C>T
ENST00000297268.10:c.793-126C>T ENSP00000297268.6:n.793-126C>T
ENST00000620463.1:c.787-126C>T ENSP00000477719.1:n.787-126C>T
NM_000089.3:c.793-126C>T , LRG_2t1:c.793-126C>T NP_000080.2:n.793-126C>T
NM_000089.4:c.793-126C>T MANE Select NP_000080.2:n.793-126C>T