Canonical Allele Identifier: CA254938135
Gene: GPC6 HGNC NCBI

Linked Data

dbSNP Id: rs550007257
MyVariant Identifiers: chr13:g.93286372A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.93286372A>C , CM000675.2:g.93286372A>C GRCh38
NC_000013.10:g.93938625A>C , CM000675.1:g.93938625A>C GRCh37
NC_000013.9:g.92736626A>C NCBI36
NG_011880.1:g.64548A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000377047.9:c.160+58756A>C MANE Select ENSP00000366246.3:n.160+58756A>C
ENST00000377047.8:c.160+58756A>C ENSP00000366246.3:n.160+58756A>C
NM_005708.3:c.160+58756A>C NP_005699.1:n.160+58756A>C
NM_005708.4:c.160+58756A>C NP_005699.1:n.160+58756A>C
XM_017020299.2:c.-51+20415A>C XP_016875788.1:n.-51+20415A>C
NM_005708.5:c.160+58756A>C MANE Select NP_005699.1:n.160+58756A>C
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