Canonical Allele Identifier: CA576321557
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1457253602
gnomAD v2: 7-94034102-A-C
gnomAD v4: 7-94404790-A-C
MyVariant Identifiers: chr7:g.94034102A>C (hg19) chr7:g.94404790A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404790A>C , CM000669.2:g.94404790A>C GRCh38
NC_000007.13:g.94034102A>C , CM000669.1:g.94034102A>C GRCh37
NC_000007.12:g.93872038A>C NCBI36
NG_007405.1:g.15230A>C , LRG_2:g.15230A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.378+44A>C MANE Select ENSP00000297268.6:n.378+44A>C
ENST00000297268.10:c.378+44A>C ENSP00000297268.6:n.378+44A>C
ENST00000620463.1:c.372+44A>C ENSP00000477719.1:n.372+44A>C
NM_000089.3:c.378+44A>C , LRG_2t1:c.378+44A>C NP_000080.2:n.378+44A>C
NM_000089.4:c.378+44A>C MANE Select NP_000080.2:n.378+44A>C
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