Canonical Allele Identifier: CA1467599739

Gene: ADAMTS3

Linked Data

• dbSNP Id: rs1719305383
• gnomAD v4: 4-72313641-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313641C>T , CM000666.2:g.72313641C>T	GRCh38
NC_000004.11:g.73179358C>T , CM000666.1:g.73179358C>T	GRCh37
NC_000004.10:g.73398222C>T	NCBI36
NG_046955.1:g.260159G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000286657.10:c.1745+36G>A MANE Select	ENSP00000286657.4:n.1745+36G>A
ENST00000286657.8:c.1745+36G>A	ENSP00000286657.4:n.1745+36G>A
ENST00000622135.1:c.1745+36G>A	ENSP00000480055.1:n.1745+36G>A
NM_014243.2:c.1745+36G>A	NP_055058.2:n.1745+36G>A
XM_011532421.1:c.1688+36G>A	XP_011530723.1:n.1688+36G>A
XM_011532422.1:c.1661+36G>A	XP_011530724.1:n.1661+36G>A
XM_011532423.1:c.1103+36G>A	XP_011530725.1:n.1103+36G>A
XM_011532424.1:c.1013+36G>A	XP_011530726.1:n.1013+36G>A
XM_011532421.2:c.1688+36G>A	XP_011530723.1:n.1688+36G>A
XM_011532422.3:c.1661+36G>A	XP_011530724.1:n.1661+36G>A
NM_014243.3:c.1745+36G>A MANE Select	NP_055058.2:n.1745+36G>A