Canonical Allele Identifier: CA1064137053
Gene: ALB HGNC NCBI

Linked Data

dbSNP Id: rs1718659427
gnomAD v3: 4-73404235-C-T
gnomAD v4: 4-73404235-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404235C>T , CM000666.2:g.73404235C>T GRCh38
NC_000004.11:g.74269952C>T , CM000666.1:g.74269952C>T GRCh37
NC_000004.10:g.74488816C>T NCBI36
NG_009291.1:g.4981C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000441319.5:c.48-134C>T ENSP00000392541.1:n.48-134C>T