Canonical Allele Identifier: CA291546981
Gene: COL1A1 HGNC NCBI

Linked Data

dbSNP Id: rs940917502
gnomAD v2: 17-48273211-G-T
gnomAD v3: 17-50195850-G-T
gnomAD v4: 17-50195850-G-T
MyVariant Identifiers: chr17:g.48273211G>T (hg19) chr17:g.50195850G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50195850G>T , CM000679.2:g.50195850G>T GRCh38
NC_000017.10:g.48273211G>T , CM000679.1:g.48273211G>T GRCh37
NC_000017.9:g.45628210G>T NCBI36
NG_007400.1:g.10790C>A , LRG_1:g.10790C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.1056+73C>A MANE Select ENSP00000225964.6:n.1056+73C>A
ENST00000225964.9:c.1056+73C>A ENSP00000225964.5:n.1056+73C>A
NM_000088.3:c.1056+73C>A , LRG_1t1:c.1056+73C>A NP_000079.2:n.1056+73C>A
XM_005257058.3:c.1056+73C>A XP_005257115.2:n.1056+73C>A
XM_005257059.3:c.957+464C>A XP_005257116.2:n.957+464C>A
XM_011524341.1:c.958-372C>A XP_011522643.1:n.958-372C>A
XM_005257058.4:c.1056+73C>A XP_005257115.2:n.1056+73C>A
XM_005257059.4:c.957+464C>A XP_005257116.2:n.957+464C>A
NM_000088.4:c.1056+73C>A MANE Select NP_000079.2:n.1056+73C>A
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