Canonical Allele Identifier: CA99696193
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs570751148
gnomAD v2: 4-74269908-C-T
gnomAD v3: 4-73404191-C-T
gnomAD v4: 4-73404191-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404191C>T , CM000666.2:g.73404191C>T GRCh38
NC_000004.11:g.74269908C>T , CM000666.1:g.74269908C>T GRCh37
NC_000004.10:g.74488772C>T NCBI36
NG_009291.1:g.4937C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000441319.5:c.48-178C>T ENSP00000392541.1:n.48-178C>T