Canonical Allele Identifier: CA449667254
Gene: C6orf47 HGNC NCBI
BAG6 HGNC NCBI

Linked Data

gnomAD v4: 6-31658342-G-T
MyVariant Identifiers: chr6:g.31626119G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31658342G>T , CM000668.2:g.31658342G>T GRCh38
NC_000006.11:g.31626119G>T , CM000668.1:g.31626119G>T GRCh37
NC_000006.10:g.31734098G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375911.2:c.*721C>A (C6orf47) MANE Select ENSP00000365076.1:n.*721C>A
ENST00000375911.1:c.*721C>A (C6orf47) ENSP00000365076.1:n.*721C>A
NM_021184.3:c.*721C>A (C6orf47) NP_067007.3:n.*721C>A
XM_011514895.1:c.-14+1979C>A (BAG6) XP_011513197.1:n.-14+1979C>A
XM_017011279.2:c.-14+1979C>A (BAG6) XP_016866768.1:n.-14+1979C>A
NM_021184.4:c.*721C>A (C6orf47) MANE Select NP_067007.3:n.*721C>A
Search 100 bp 5'
Search 100 bp 3'