Canonical Allele Identifier: CA357241336

Gene: ALB

Linked Data

• dbSNP Id: rs1718980918
• gnomAD v4: 4-73415115-C-T
• MyVariant Identifiers: chr4:g.74280832C>T (hg19) ; chr4:g.73415115C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415115C>T , CM000666.2:g.73415115C>T	GRCh38
NC_000004.11:g.74280832C>T , CM000666.1:g.74280832C>T	GRCh37
NC_000004.10:g.74499696C>T	NCBI36
NG_009291.1:g.15861C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1139C>T MANE Select	ENSP00000295897.4:p.Thr380Ile
ENST00000295897.8:c.1139C>T	ENSP00000295897.4:p.Thr380Ile
ENST00000401494.7:c.794C>T	ENSP00000384695.3:p.Thr265Ile
ENST00000415165.6:c.563C>T	ENSP00000401820.2:p.Thr188Ile
ENST00000476441.6:c.*418C>T	ENSP00000423727.1:n.*418C>T
ENST00000484992.1:n.459C>T
ENST00000503124.5:c.689C>T	ENSP00000421027.1:p.Thr230Ile
ENST00000504043.1:n.142C>T
ENST00000505649.5:n.825C>T
ENST00000509063.5:c.1139C>T	ENSP00000422784.1:p.Thr380Ile
ENST00000511370.1:c.672C>T
ENST00000621085.4:c.500C>T	ENSP00000483421.1:p.Thr167Ile
ENST00000621628.4:c.500C>T	ENSP00000480485.1:p.Thr167Ile
NM_000477.5:c.1139C>T	NP_000468.1:p.Thr380Ile
NM_000477.6:c.1139C>T	NP_000468.1:p.Thr380Ile
NM_000477.7:c.1139C>T MANE Select	NP_000468.1:p.Thr380Ile