Canonical Allele Identifier: CA291547474
Gene: COL1A1 HGNC NCBI

Linked Data

dbSNP Id: rs2696248
MyVariant Identifiers: chr17:g.48274246T>G (hg19) chr17:g.50196885T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50196885T>G , CM000679.2:g.50196885T>G GRCh38
NC_000017.10:g.48274246T>G , CM000679.1:g.48274246T>G GRCh37
NC_000017.9:g.45629245T>G NCBI36
NG_007400.1:g.9755A>C , LRG_1:g.9755A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.804+125A>C MANE Select ENSP00000225964.6:n.804+125A>C
ENST00000225964.9:c.804+125A>C ENSP00000225964.5:n.804+125A>C
ENST00000495677.1:n.531+125A>C
NM_000088.3:c.804+125A>C , LRG_1t1:c.804+125A>C NP_000079.2:n.804+125A>C
XM_005257058.3:c.804+125A>C XP_005257115.2:n.804+125A>C
XM_005257059.3:c.804+125A>C XP_005257116.2:n.804+125A>C
XM_011524341.1:c.804+125A>C XP_011522643.1:n.804+125A>C
XM_005257058.4:c.804+125A>C XP_005257115.2:n.804+125A>C
XM_005257059.4:c.804+125A>C XP_005257116.2:n.804+125A>C
NM_000088.4:c.804+125A>C MANE Select NP_000079.2:n.804+125A>C
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