Canonical Allele Identifier: CA254938137
Gene: GPC6 HGNC NCBI

Linked Data

dbSNP Id: rs896137173
gnomAD v3: 13-93286378-T-G
gnomAD v4: 13-93286378-T-G
MyVariant Identifiers: chr13:g.93938631T>G (hg19) chr13:g.93286378T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.93286378T>G , CM000675.2:g.93286378T>G GRCh38
NC_000013.10:g.93938631T>G , CM000675.1:g.93938631T>G GRCh37
NC_000013.9:g.92736632T>G NCBI36
NG_011880.1:g.64554T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000377047.9:c.160+58762T>G MANE Select ENSP00000366246.3:n.160+58762T>G
ENST00000377047.8:c.160+58762T>G ENSP00000366246.3:n.160+58762T>G
NM_005708.3:c.160+58762T>G NP_005699.1:n.160+58762T>G
NM_005708.4:c.160+58762T>G NP_005699.1:n.160+58762T>G
XM_017020299.2:c.-51+20421T>G XP_016875788.1:n.-51+20421T>G
NM_005708.5:c.160+58762T>G MANE Select NP_005699.1:n.160+58762T>G
Search 100 bp 5'
Search 100 bp 3'