Canonical Allele Identifier: CA500849517
Gene: COL1A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48271940A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194579A>C , CM000679.2:g.50194579A>C GRCh38
NC_000017.10:g.48271940A>C , CM000679.1:g.48271940A>C GRCh37
NC_000017.9:g.45626939A>C NCBI36
NG_007400.1:g.12061T>G , LRG_1:g.12061T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1509T>G MANE Select ENSP00000225964.6:p.Gly503=
ENST00000225964.9:c.1509T>G ENSP00000225964.5:p.Gly503=
ENST00000471344.1:n.453T>G
NM_000088.3:c.1509T>G , LRG_1t1:c.1509T>G NP_000079.2:p.Gly503=
XM_005257058.3:c.1509T>G XP_005257115.2:p.Gly503=
XM_005257059.3:c.957+1735T>G XP_005257116.2:n.957+1735T>G
XM_011524341.1:c.1311T>G XP_011522643.1:p.Gly437=
XM_005257058.4:c.1509T>G XP_005257115.2:p.Gly503=
XM_005257059.4:c.957+1735T>G XP_005257116.2:n.957+1735T>G
NM_000088.4:c.1509T>G MANE Select NP_000079.2:p.Gly503=