Canonical Allele Identifier: CA357241574

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280873T>C (hg19) ; chr4:g.73415156T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415156T>C , CM000666.2:g.73415156T>C	GRCh38
NC_000004.11:g.74280873T>C , CM000666.1:g.74280873T>C	GRCh37
NC_000004.10:g.74499737T>C	NCBI36
NG_009291.1:g.15902T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1180T>C MANE Select	ENSP00000295897.4:p.Tyr394His
ENST00000295897.8:c.1180T>C	ENSP00000295897.4:p.Tyr394His
ENST00000401494.7:c.835T>C	ENSP00000384695.3:p.Tyr279His
ENST00000415165.6:c.604T>C	ENSP00000401820.2:p.Tyr202His
ENST00000476441.6:c.*459T>C	ENSP00000423727.1:n.*459T>C
ENST00000484992.1:n.500T>C
ENST00000503124.5:c.730T>C	ENSP00000421027.1:p.Tyr244His
ENST00000504043.1:n.183T>C
ENST00000505649.5:n.866T>C
ENST00000509063.5:c.1180T>C	ENSP00000422784.1:p.Tyr394His
ENST00000511370.1:c.713T>C
ENST00000621085.4:c.541T>C	ENSP00000483421.1:p.Tyr181His
ENST00000621628.4:c.541T>C	ENSP00000480485.1:p.Tyr181His
NM_000477.5:c.1180T>C	NP_000468.1:p.Tyr394His
NM_000477.6:c.1180T>C	NP_000468.1:p.Tyr394His
NM_000477.7:c.1180T>C MANE Select	NP_000468.1:p.Tyr394His