Canonical Allele Identifier: CA357234626

Gene: ALB

Linked Data

• dbSNP Id: rs763075976
• gnomAD v2: 4-74270100-G-C
• gnomAD v4: 4-73404383-G-C
• MyVariant Identifiers: chr4:g.74270100G>C (hg19) ; chr4:g.73404383G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404383G>C , CM000666.2:g.73404383G>C	GRCh38
NC_000004.11:g.74270100G>C , CM000666.1:g.74270100G>C	GRCh37
NC_000004.10:g.74488964G>C	NCBI36
NG_009291.1:g.5129G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.56G>C MANE Select	ENSP00000295897.4:p.Arg19Thr
ENST00000295897.8:c.56G>C	ENSP00000295897.4:p.Arg19Thr
ENST00000401494.7:c.56G>C	ENSP00000384695.3:p.Arg19Thr
ENST00000415165.6:c.56G>C	ENSP00000401820.2:p.Arg19Thr
ENST00000441319.5:c.62G>C	ENSP00000392541.1:p.Arg21Thr
ENST00000476441.6:c.56G>C	ENSP00000423727.1:p.Arg19Thr
ENST00000503124.5:c.-125G>C	ENSP00000421027.1:n.-125G>C
ENST00000509063.5:c.56G>C	ENSP00000422784.1:p.Arg19Thr
ENST00000510166.5:n.97G>C
ENST00000514786.1:n.48+47G>C
ENST00000515133.5:n.97G>C
ENST00000621085.4:c.56G>C	ENSP00000483421.1:p.Arg19Thr
ENST00000621628.4:c.56G>C	ENSP00000480485.1:p.Arg19Thr
NM_000477.5:c.56G>C	NP_000468.1:p.Arg19Thr
NM_000477.6:c.56G>C	NP_000468.1:p.Arg19Thr
NM_000477.7:c.56G>C MANE Select	NP_000468.1:p.Arg19Thr