Canonical Allele Identifier: CA3045112721

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404320T>C , CM000666.2:g.73404320T>C	GRCh38
NC_000004.11:g.74270037T>C , CM000666.1:g.74270037T>C	GRCh37
NC_000004.10:g.74488901T>C	NCBI36
NG_009291.1:g.5066T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.-8T>C MANE Select	ENSP00000295897.4:n.-8T>C
ENST00000295897.8:c.-8T>C	ENSP00000295897.4:n.-8T>C
ENST00000401494.7:c.-8T>C	ENSP00000384695.3:n.-8T>C
ENST00000415165.6:c.-8T>C	ENSP00000401820.2:n.-8T>C
ENST00000441319.5:c.48-49T>C	ENSP00000392541.1:n.48-49T>C
ENST00000476441.6:c.-8T>C	ENSP00000423727.1:n.-8T>C
ENST00000503124.5:c.-188T>C	ENSP00000421027.1:n.-188T>C
ENST00000509063.5:c.-8T>C	ENSP00000422784.1:n.-8T>C
ENST00000510166.5:n.34T>C
ENST00000514786.1:n.32T>C
ENST00000515133.5:n.34T>C
ENST00000621085.4:c.-8T>C	ENSP00000483421.1:n.-8T>C
ENST00000621628.4:c.-8T>C	ENSP00000480485.1:n.-8T>C
NM_000477.5:c.-8T>C	NP_000468.1:n.-8T>C
NM_000477.6:c.-8T>C	NP_000468.1:n.-8T>C
NM_000477.7:c.-8T>C MANE Select	NP_000468.1:n.-8T>C