Canonical Allele Identifier: CA075927
Gene: COL3A1 HGNC NCBI

Linked Data

dbSNP Id: rs747224512
ExAC: 2:189871635 T / A
gnomAD v2: 2-189871635-T-A
gnomAD v3: 2-189006909-T-A
gnomAD v4: 2-189006909-T-A
MyVariant Identifiers: chr2:g.189871635T>A (hg19) chr2:g.189006909T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189006909T>A , CM000664.2:g.189006909T>A GRCh38
NC_000002.11:g.189871635T>A , CM000664.1:g.189871635T>A GRCh37
NC_000002.10:g.189579880T>A NCBI36
NG_007404.1:g.37537T>A , LRG_3:g.37537T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000450867.2:c.3103-28T>A ENSP00000415346.2:n.3103-28T>A
ENST00000304636.9:c.3202-28T>A MANE Select ENSP00000304408.4:n.3202-28T>A
ENST00000304636.7:c.3202-28T>A ENSP00000304408.3:n.3202-28T>A
ENST00000317840.9:c.2528-1145T>A ENSP00000315243.6:n.2528-1145T>A
NM_000090.3:c.3202-28T>A , LRG_3t1:c.3202-28T>A NP_000081.1:n.3202-28T>A
NM_000090.4:c.3202-28T>A MANE Select NP_000081.2:n.3202-28T>A
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