Canonical Allele Identifier: CA62557158
Gene: COL3A1 HGNC NCBI

Linked Data

dbSNP Id: rs898263769
gnomAD v3: 2-189003883-C-G
gnomAD v4: 2-189003883-C-G
MyVariant Identifiers: chr2:g.189868609C>G (hg19) chr2:g.189003883C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189003883C>G , CM000664.2:g.189003883C>G GRCh38
NC_000002.11:g.189868609C>G , CM000664.1:g.189868609C>G GRCh37
NC_000002.10:g.189576854C>G NCBI36
NG_007404.1:g.34511C>G , LRG_3:g.34511C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000450867.2:c.2562+96C>G ENSP00000415346.2:n.2562+96C>G
ENST00000304636.9:c.2661+96C>G MANE Select ENSP00000304408.4:n.2661+96C>G
ENST00000304636.7:c.2661+96C>G ENSP00000304408.3:n.2661+96C>G
ENST00000317840.9:c.2527+847C>G ENSP00000315243.6:n.2527+847C>G
ENST00000467886.1:n.192C>G
NM_000090.3:c.2661+96C>G , LRG_3t1:c.2661+96C>G NP_000081.1:n.2661+96C>G
NM_000090.4:c.2661+96C>G MANE Select NP_000081.2:n.2661+96C>G
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