Canonical Allele Identifier: CA2683768128
Gene: COL1A2 HGNC NCBI

Linked Data

gnomAD v4: 7-94409200-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94409200T>A , CM000669.2:g.94409200T>A GRCh38
NC_000007.13:g.94038512T>A , CM000669.1:g.94038512T>A GRCh37
NC_000007.12:g.93876448T>A NCBI36
NG_007405.1:g.19640T>A , LRG_2:g.19640T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.793-122T>A MANE Select ENSP00000297268.6:n.793-122T>A
ENST00000297268.10:c.793-122T>A ENSP00000297268.6:n.793-122T>A
ENST00000620463.1:c.787-122T>A ENSP00000477719.1:n.787-122T>A
NM_000089.3:c.793-122T>A , LRG_2t1:c.793-122T>A NP_000080.2:n.793-122T>A
NM_000089.4:c.793-122T>A MANE Select NP_000080.2:n.793-122T>A
Search 100 bp 5'
Search 100 bp 3'