Canonical Allele Identifier: CA2677984647
Gene: C6orf47 HGNC NCBI
BAG6 HGNC NCBI

Linked Data

gnomAD v4: 6-31658327-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31658327A>G , CM000668.2:g.31658327A>G GRCh38
NC_000006.11:g.31626104A>G , CM000668.1:g.31626104A>G GRCh37
NC_000006.10:g.31734083A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375911.2:c.*736T>C (C6orf47) MANE Select ENSP00000365076.1:n.*736T>C
ENST00000375911.1:c.*736T>C (C6orf47) ENSP00000365076.1:n.*736T>C
NM_021184.3:c.*736T>C (C6orf47) NP_067007.3:n.*736T>C
XM_011514895.1:c.-14+1994T>C (BAG6) XP_011513197.1:n.-14+1994T>C
XM_017011279.2:c.-14+1994T>C (BAG6) XP_016866768.1:n.-14+1994T>C
NM_021184.4:c.*736T>C (C6orf47) MANE Select NP_067007.3:n.*736T>C