Canonical Allele Identifier: CA99696233
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs983703538
gnomAD v3: 4-73404193-G-T
gnomAD v4: 4-73404193-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404193G>T , CM000666.2:g.73404193G>T GRCh38
NC_000004.11:g.74269910G>T , CM000666.1:g.74269910G>T GRCh37
NC_000004.10:g.74488774G>T NCBI36
NG_009291.1:g.4939G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-176G>T ENSP00000392541.1:n.48-176G>T