Canonical Allele Identifier: CA162919418
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs974194865
gnomAD v2: 7-94038537-G-T
gnomAD v3: 7-94409225-G-T
gnomAD v4: 7-94409225-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94409225G>T , CM000669.2:g.94409225G>T GRCh38
NC_000007.13:g.94038537G>T , CM000669.1:g.94038537G>T GRCh37
NC_000007.12:g.93876473G>T NCBI36
NG_007405.1:g.19665G>T , LRG_2:g.19665G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.793-97G>T MANE Select ENSP00000297268.6:n.793-97G>T
ENST00000297268.10:c.793-97G>T ENSP00000297268.6:n.793-97G>T
ENST00000620463.1:c.787-97G>T ENSP00000477719.1:n.787-97G>T
NM_000089.3:c.793-97G>T , LRG_2t1:c.793-97G>T NP_000080.2:n.793-97G>T
NM_000089.4:c.793-97G>T MANE Select NP_000080.2:n.793-97G>T