Canonical Allele Identifier: CA449667256
Gene: C6orf47 HGNC NCBI
BAG6 HGNC NCBI

Linked Data

gnomAD v4: 6-31658343-T-C
MyVariant Identifiers: chr6:g.31626120T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31658343T>C , CM000668.2:g.31658343T>C GRCh38
NC_000006.11:g.31626120T>C , CM000668.1:g.31626120T>C GRCh37
NC_000006.10:g.31734099T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375911.2:c.*720A>G (C6orf47) MANE Select ENSP00000365076.1:n.*720A>G
ENST00000375911.1:c.*720A>G (C6orf47) ENSP00000365076.1:n.*720A>G
NM_021184.3:c.*720A>G (C6orf47) NP_067007.3:n.*720A>G
XM_011514895.1:c.-14+1978A>G (BAG6) XP_011513197.1:n.-14+1978A>G
XM_017011279.2:c.-14+1978A>G (BAG6) XP_016866768.1:n.-14+1978A>G
NM_021184.4:c.*720A>G (C6orf47) MANE Select NP_067007.3:n.*720A>G