Canonical Allele Identifier: CA365416899
Gene: FAM162B HGNC NCBI

Linked Data

dbSNP Id: rs654128
MyVariant Identifiers: chr6:g.117086378C>G (hg19) chr6:g.116765215C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.116765215C>G , CM000668.2:g.116765215C>G GRCh38
NC_000006.11:g.117086378C>G , CM000668.1:g.117086378C>G GRCh37
NC_000006.10:g.117193071C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368557.6:c.213G>C MANE Select ENSP00000357545.4:p.Gln71His
ENST00000368557.5:c.213G>C ENSP00000357545.4:p.Gln71His
NM_001085480.2:c.213G>C NP_001078949.1:p.Gln71His
NM_001085480.3:c.213G>C MANE Select NP_001078949.1:p.Gln71His
Search 100 bp 5'
Search 100 bp 3'