Canonical Allele Identifier: CA2683773838
Gene: COL1A2 HGNC NCBI

Linked Data

gnomAD v4: 7-94426625-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94426625G>T , CM000669.2:g.94426625G>T GRCh38
NC_000007.13:g.94055937G>T , CM000669.1:g.94055937G>T GRCh37
NC_000007.12:g.93893873G>T NCBI36
NG_007405.1:g.37065G>T , LRG_2:g.37065G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.3105+95G>T MANE Select ENSP00000297268.6:n.3105+95G>T
ENST00000297268.10:c.3105+95G>T ENSP00000297268.6:n.3105+95G>T
ENST00000478215.1:n.759G>T
ENST00000481570.5:n.3173G>T
ENST00000488121.1:n.21+95G>T
ENST00000620463.1:c.3099+95G>T ENSP00000477719.1:n.3099+95G>T
NM_000089.3:c.3105+95G>T , LRG_2t1:c.3105+95G>T NP_000080.2:n.3105+95G>T
NM_000089.4:c.3105+95G>T MANE Select NP_000080.2:n.3105+95G>T