Canonical Allele Identifier: CA98747696
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs979916375
gnomAD v2: 4-69512610-T-C
gnomAD v3: 4-68646892-T-C
gnomAD v4: 4-68646892-T-C
MyVariant Identifiers: chr4:g.69512610T>C (hg19) chr4:g.68646892T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646892T>C , CM000666.2:g.68646892T>C GRCh38
NC_000004.11:g.69512610T>C , CM000666.1:g.69512610T>C GRCh37
NC_000004.10:g.69195205T>C NCBI36
NG_052676.1:g.28885A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*212A>G MANE Select ENSP00000341045.5:n.*212A>G
ENST00000338206.5:c.*212A>G ENSP00000341045.5:n.*212A>G
ENST00000616841.4:c.1732+73A>G ENSP00000482004.1:n.1732+73A>G
NM_001076.3:c.*212A>G NP_001067.2:n.*212A>G
NM_001076.4:c.*212A>G MANE Select NP_001067.2:n.*212A>G
Search 100 bp 5'
Search 100 bp 3'