Canonical Allele Identifier: CA137538710
Gene: MDGA1 HGNC NCBI

Linked Data

dbSNP Id: rs1883901
gnomAD v2: 6-37631031-G-A
gnomAD v3: 6-37663255-G-A
gnomAD v4: 6-37663255-G-A
MyVariant Identifiers: chr6:g.37631031G>A (hg19) chr6:g.37663255G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.37663255G>A , CM000668.2:g.37663255G>A GRCh38
NC_000006.11:g.37631031G>A , CM000668.1:g.37631031G>A GRCh37
NC_000006.10:g.37739009G>A NCBI36
NG_051764.1:g.39736C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000434837.8:c.207+712C>T MANE Select ENSP00000402584.2:n.207+712C>T
ENST00000650466.1:c.207+712C>T ENSP00000498018.1:n.207+712C>T
ENST00000681439.1:c.39+712C>T ENSP00000506441.1:n.39+712C>T
ENST00000681472.1:c.207+712C>T ENSP00000506519.1:n.207+712C>T
ENST00000434837.7:c.207+712C>T ENSP00000402584.2:n.207+712C>T
ENST00000478143.2:n.23+712C>T
ENST00000505425.5:c.207+712C>T ENSP00000422042.1:n.207+712C>T
ENST00000508399.1:c.39+712C>T ENSP00000427645.1:n.39+712C>T
ENST00000515437.5:c.39+712C>T ENSP00000421510.1:n.39+712C>T
NM_153487.3:c.207+712C>T NP_705691.1:n.207+712C>T
XM_006715056.2:c.207+712C>T XP_006715119.1:n.207+712C>T
XM_006715057.2:c.207+712C>T XP_006715120.1:n.207+712C>T
XR_926140.1:n.396+712C>T
XR_926141.1:n.396+712C>T
XR_926142.1:n.396+712C>T
XM_006715056.3:c.207+712C>T XP_006715119.1:n.207+712C>T
XM_017010734.1:c.207+712C>T XP_016866223.1:n.207+712C>T
XR_926140.2:n.330+712C>T
XR_926141.2:n.330+712C>T
XR_926142.2:n.330+712C>T
NM_153487.4:c.207+712C>T MANE Select NP_705691.1:n.207+712C>T
Search 100 bp 5'
Search 100 bp 3'