Canonical Allele Identifier: CA99696451

Gene: ALB

Linked Data

• dbSNP Id: rs978356536
• gnomAD v2: 4-74270101-G-T
• gnomAD v4: 4-73404384-G-T
• MyVariant Identifiers: chr4:g.74270101G>T (hg19) ; chr4:g.73404384G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404384G>T , CM000666.2:g.73404384G>T	GRCh38
NC_000004.11:g.74270101G>T , CM000666.1:g.74270101G>T	GRCh37
NC_000004.10:g.74488965G>T	NCBI36
NG_009291.1:g.5130G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.57G>T MANE Select	ENSP00000295897.4:p.Arg19Ser
ENST00000295897.8:c.57G>T	ENSP00000295897.4:p.Arg19Ser
ENST00000401494.7:c.57G>T	ENSP00000384695.3:p.Arg19Ser
ENST00000415165.6:c.57G>T	ENSP00000401820.2:p.Arg19Ser
ENST00000441319.5:c.63G>T	ENSP00000392541.1:p.Arg21Ser
ENST00000476441.6:c.57G>T	ENSP00000423727.1:p.Arg19Ser
ENST00000503124.5:c.-124G>T	ENSP00000421027.1:n.-124G>T
ENST00000509063.5:c.57G>T	ENSP00000422784.1:p.Arg19Ser
ENST00000510166.5:n.98G>T
ENST00000514786.1:n.48+48G>T
ENST00000515133.5:n.98G>T
ENST00000621085.4:c.57G>T	ENSP00000483421.1:p.Arg19Ser
ENST00000621628.4:c.57G>T	ENSP00000480485.1:p.Arg19Ser
NM_000477.5:c.57G>T	NP_000468.1:p.Arg19Ser
NM_000477.6:c.57G>T	NP_000468.1:p.Arg19Ser
NM_000477.7:c.57G>T MANE Select	NP_000468.1:p.Arg19Ser